Atropine Sulfate


Bausch & Lomb Incorporated
Human Prescription Drug
NDC 24208-965
Atropine Sulfate is a human prescription drug labeled by 'Bausch & Lomb Incorporated'. National Drug Code (NDC) number for Atropine Sulfate is 24208-965. This drug is available in dosage form of Solution. The names of the active, medicinal ingredients in Atropine Sulfate drug includes Atropine Sulfate - 10 mg/mL . The currest status of Atropine Sulfate drug is Active.

Drug Information:

Drug NDC: 24208-965
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Atropine Sulfate
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Atropine Sulfate
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Bausch & Lomb Incorporated
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Solution
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:ATROPINE SULFATE - 10 mg/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:OPHTHALMIC
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: NDA
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 13 Jul, 2022
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 21 Jun, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: NDA213581
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Bausch & Lomb Incorporated
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:1190655
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UNII:03J5ZE7KA5
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:Anticholinergic [EPC]
Cholinergic Antagonists [MoA]
Cholinergic Muscarinic Antagonist [EPC]
Cholinergic Muscarinic Antagonists [MoA]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
24208-965-0110 VIAL in 1 CARTON (24208-965-01) / .4 mL in 1 VIAL13 Jul, 2022N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Product Elements:

Atropine sulfate atropine sulfate atropine sulfate atropine boric acid hydrochloric acid sodium hydroxide water hypromellose, unspecified

Drug Interactions:

7 drug interactions the use of atropine and monoamine oxidase inhibitors (maoi) is generally not recommended because of the potential to precipitate hypertensive crisis ( 7 ). 7.1 monoamine oxidase inhibitors (maoi) the use of atropine and monoamine oxidase inhibitors (maoi) is generally not recommended because of the potential to precipitate hypertensive crisis.

Indications and Usage:

1 indications and usage atropine sulfate ophthalmic solution, usp 1% is indicated for: atropine is an anti-muscarinic agent indicated for: • mydriasis ( 1.1 ) • cycloplegia ( 1.2 ) • penalization of the healthy eye in the treatment of amblyopia ( 1.3 ) 1.1 mydriasis 1.2 cycloplegia 1.3 penalization of the healthy eye in the treatment of amblyopia

Warnings and Cautions:

5 warnings and precautions • photophobia and blurred vision due to pupil unresponsiveness and cycloplegia may last up to 2 weeks ( 5.1 ). • risk of blood pressure increase from systemic absorption ( 5.2 ). • to avoid the potential for eye injury or contamination, care should be taken to avoid touching the single-dose vial to the eye or to any other surface ( 5.3 ). 5.1 photophobia and blurred vision photophobia and blurred vision due to pupil unresponsiveness and cycloplegia may last up to 2 weeks. 5.2 elevation of blood pressure elevation in blood pressure from systemic absorption has been reported following conjunctival instillation of recommended doses of atropine sulfate ophthalmic solution, usp 1%. 5.3 potential for eye injury or contamination to avoid the potential for eye injury or contamination, care should be taken to avoid touching the single-dose vial to the eye or to any other surface.

Dosage and Administration:

2 dosage and administration in individuals from three (3) months of age or greater, 1 drop topically to the cul-de-sac of the conjunctiva in one or both eyes as indicated, forty minutes prior to the intended maximal dilation time. in individuals 3 years of age or greater, doses may be repeated up to twice daily as needed. discard the single-dose vial immediately after use in one or both eyes. • in individuals from three (3) months of age or greater, 1 drop topically to the cul-de-sac of the conjunctiva, forty minutes prior to the intended maximal dilation time (2.1). • in individuals 3 years of age or greater, doses may be repeated up to twice daily as needed (2.2).

Dosage Forms and Strength:

3 dosage forms and strengths atropine sulfate ophthalmic solution, usp 1%: each ml contains 10 mg of atropine sulfate. ophthalmic solution: 1% atropine sulfate (10 mg/ml) ( 3 ).

Contraindications:

4 contraindications atropine sulfate ophthalmic solution, usp 1% should not be used in anyone who has demonstrated a previous hypersensitivity or known allergic reaction to any ingredient of the formulation because it may recur. hypersensitivity or allergic reaction to any ingredient in the formulation ( 4 ).

Adverse Reactions:

6 adverse reactions the following serious adverse reactions are described below and elsewhere in the labeling: • photophobia and blurred vision [see warnings and precautions (5.1) ] • elevation in blood pressure [see warnings and precautions (5.2) ] the following adverse reactions have been identified following use of atropine sulfate ophthalmic solution. because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. most common adverse reactions that have been reported are eye pain and stinging on administration, blurred vision, photophobia, superficial keratitis, decreased lacrimation, drowsiness, increased heart rate and blood pressure ( 6 ). to report suspected adverse reactions, contact bausch & lomb incorporated at 1-800-553-5340 or fda at 1-800-fda-1088 or www.fda.gov/medwatch. 6.1 ocular adverse reactions eye pain and stinging occu
rs upon instillation of atropine sulfate ophthalmic solution. other commonly occurring adverse reactions include blurred vision, photophobia, superficial keratitis and decreased lacrimation. allergic reactions such as papillary conjunctivitis, contact dermatitis, and eyelid edema may also occur less commonly. 6.2 systemic adverse reactions systemic effects of atropine are related to its anti-muscarinic activity. systemic adverse events reported include dryness of skin, mouth, and throat from decreased secretions from mucous membranes; drowsiness, restlessness, irritability or delirium from stimulation of the central nervous system; tachycardia; flushed skin of the face and neck.

Drug Interactions:

7 drug interactions the use of atropine and monoamine oxidase inhibitors (maoi) is generally not recommended because of the potential to precipitate hypertensive crisis ( 7 ). 7.1 monoamine oxidase inhibitors (maoi) the use of atropine and monoamine oxidase inhibitors (maoi) is generally not recommended because of the potential to precipitate hypertensive crisis.

Use in Specific Population:

8 use in specific populations 8.1 pregnancy risk summary there are no adequate and well-controlled studies of atropine sulfate ophthalmic solution, usp 1% administration in pregnant women to inform a drug-associated risk. adequate animal development and reproduction studies have not been conducted with atropine sulfate. in humans, 1% atropine sulfate is systemically bioavailable following topical ocular administration [see clinical pharmacology (12.3) ] . atropine sulfate ophthalmic solution, usp 1% should only be used during pregnancy if the potential benefit justifies the potential risk to the fetus. 8.2 lactation risk summary there is no information to inform risk regarding the presence of atropine in human milk following ocular administrations of atropine sulfate ophthalmic solution, usp 1% to the mother. the effects on breastfed infants and the effects on milk production are also unknown. the developmental and health benefits of breastfeeding should be considered along with the mo
ther’s clinical need for atropine sulfate ophthalmic solution, usp 1% and any potential adverse effects on the breastfed child from atropine sulfate ophthalmic solution, usp 1%. 8.4 pediatric use due to the potential for systemic absorption, the use of atropine sulfate ophthalmic solution, usp 1% in children under the age of 3 months is not recommended and the use in children under 3 years of age should be limited to no more than one drop per eye per day. safety and efficacy in children above the age of 3 months has been established in adequate and well controlled trials. 8.5 geriatric use no overall differences in safety and effectiveness have been observed between elderly and younger adult patients.

Use in Pregnancy:

8.1 pregnancy risk summary there are no adequate and well-controlled studies of atropine sulfate ophthalmic solution, usp 1% administration in pregnant women to inform a drug-associated risk. adequate animal development and reproduction studies have not been conducted with atropine sulfate. in humans, 1% atropine sulfate is systemically bioavailable following topical ocular administration [see clinical pharmacology (12.3) ] . atropine sulfate ophthalmic solution, usp 1% should only be used during pregnancy if the potential benefit justifies the potential risk to the fetus.

Pediatric Use:

8.4 pediatric use due to the potential for systemic absorption, the use of atropine sulfate ophthalmic solution, usp 1% in children under the age of 3 months is not recommended and the use in children under 3 years of age should be limited to no more than one drop per eye per day. safety and efficacy in children above the age of 3 months has been established in adequate and well controlled trials.

Geriatric Use:

8.5 geriatric use no overall differences in safety and effectiveness have been observed between elderly and younger adult patients.

Overdosage:

10 overdosage in the event of accidental ingestion or toxic overdosage with atropine sulfate ophthalmic solution, usp 1%, supportive care may include a short acting barbiturate or diazepam as needed to control marked excitement and convulsions. large doses for sedation should be avoided because central depressant action may coincide with the depression occurring late in atropine poisoning. central stimulants are not recommended. physostigmine, given by slow intravenous injection of 1 to 4 mg (0.5 to 1 mg in pediatric populations), rapidly abolishes delirium and coma caused by large doses of atropine. since physostigmine is rapidly destroyed, the patient may again lapse into coma after one to two hours, and repeated doses may be required. artificial respiration with oxygen may be necessary. cooling measures may be needed to help to reduce fever, especially in pediatric populations. the fatal adult dose of atropine is not known. in pediatric populations, 10 mg or less may be fatal.

Description:

11 description atropine sulfate ophthalmic solution, usp 1% is an aseptically prepared, sterile solution for topical ophthalmic use. the product does not contain an antimicrobial preservative. the active ingredient is represented by the chemical structure: chemical name: benzeneacetic acid, α-(hydroxymethyl)-, 8-methyl-8-azabicyclo[3.2.1.]oct-3-yl ester, endo –(±)-, sulfate (2:1) (salt), monohydrate. molecular formula: (c 17 h 23 no 3 ) 2 • h 2 so 4 • h 2 o molecular weight: 694.84 g/mol each ml of atropine sulfate ophthalmic solution, usp 1% contains: active: atropine sulfate 10 mg equivalent to 8.3 mg of atropine. inactives: boric acid, hydroxypropyl methylcellulose, hydrochloric acid and/or sodium hydroxide may be added to adjust ph (3.5 to 6.0), and water for injection usp. chemstructure

Clinical Pharmacology:

12 clinical pharmacology 12.1 mechanism of action atropine is a reversible antagonist of muscarine-like actions of acetylcholine and is therefore classified as an anti-muscarinic agent. atropine is relatively selective for muscarinic receptors. its potency at nicotinic receptors is much lower, and actions at non-muscarinic receptors are generally undetectable clinically. atropine does not distinguish among the m1, m2, and m3 subgroups of muscarinic receptors. the pupillary constrictor muscle depends on muscarinic cholinoceptor activation. this activation is blocked by topical atropine resulting in unopposed sympathetic dilator activity and mydriasis. atropine also weakens the contraction of the ciliary muscle, or cycloplegia. cycloplegia results in loss of the ability to accommodate such that the eye cannot focus for near vision. 12.2 pharmacodynamics the onset of action after administration of atropine sulfate ophthalmic solution, usp 1% generally occurs within minutes with maximal ef
fect seen in hours and the effect can last multiple days [see clinical studies (14) ] . 12.3 pharmacokinetics in a study of healthy subjects, after topical ocular administration of 30 μl of atropine sulfate ophthalmic solution 1%, the mean (± sd) systemic bioavailability of l-hyoscyamine was reported to be approximately 64 ± 29% (range 19% to 95%) as compared to intravenous administration of atropine sulfate. the median (range) time to maximum plasma concentration (tmax) was 19 minutes (range 3 to 60 minutes), and the mean (±sd) peak plasma concentration (cmax) of l-hyoscyamine was 288 ± 73 pg/ml. the mean (±sd) plasma half-life was reported to be approximately 2.5 ± 0.8 hours. in a separate study of patients undergoing ocular surgery, after topical ocular administration of 40 μl of atropine sulfate ophthalmic solution, 1%, the mean (± sd) plasma cmax of l-hyoscyamine was 860 ± 402 pg/ml, which was observed within 8 minutes following administration.

Mechanism of Action:

12.1 mechanism of action atropine is a reversible antagonist of muscarine-like actions of acetylcholine and is therefore classified as an anti-muscarinic agent. atropine is relatively selective for muscarinic receptors. its potency at nicotinic receptors is much lower, and actions at non-muscarinic receptors are generally undetectable clinically. atropine does not distinguish among the m1, m2, and m3 subgroups of muscarinic receptors. the pupillary constrictor muscle depends on muscarinic cholinoceptor activation. this activation is blocked by topical atropine resulting in unopposed sympathetic dilator activity and mydriasis. atropine also weakens the contraction of the ciliary muscle, or cycloplegia. cycloplegia results in loss of the ability to accommodate such that the eye cannot focus for near vision.

Pharmacodynamics:

12.2 pharmacodynamics the onset of action after administration of atropine sulfate ophthalmic solution, usp 1% generally occurs within minutes with maximal effect seen in hours and the effect can last multiple days [see clinical studies (14) ] .

Pharmacokinetics:

12.3 pharmacokinetics in a study of healthy subjects, after topical ocular administration of 30 μl of atropine sulfate ophthalmic solution 1%, the mean (± sd) systemic bioavailability of l-hyoscyamine was reported to be approximately 64 ± 29% (range 19% to 95%) as compared to intravenous administration of atropine sulfate. the median (range) time to maximum plasma concentration (tmax) was 19 minutes (range 3 to 60 minutes), and the mean (±sd) peak plasma concentration (cmax) of l-hyoscyamine was 288 ± 73 pg/ml. the mean (±sd) plasma half-life was reported to be approximately 2.5 ± 0.8 hours. in a separate study of patients undergoing ocular surgery, after topical ocular administration of 40 μl of atropine sulfate ophthalmic solution, 1%, the mean (± sd) plasma cmax of l-hyoscyamine was 860 ± 402 pg/ml, which was observed within 8 minutes following administration.

Nonclinical Toxicology:

13 nonclinical toxicology 13.1 carcinogenesis, mutagenesis, impairment of fertility atropine sulfate was negative in the salmonella /microsome mutagenicity test. studies to evaluate carcinogenicity and impairment of fertility have not been conducted.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

13.1 carcinogenesis, mutagenesis, impairment of fertility atropine sulfate was negative in the salmonella /microsome mutagenicity test. studies to evaluate carcinogenicity and impairment of fertility have not been conducted.

Clinical Studies:

14 clinical studies topical administration of atropine sulfate ophthalmic solution, usp 1% results in mydriasis and/or cycloplegia with efficacy demonstrated in both adults and children. the maximum effect for mydriasis is achieved in about 30–40 minutes after administration, with recovery after approximately 7–10 days. the maximum effect for cycloplegia is achieved within 60–180 minutes after administration, with recovery after approximately 7–12 days.

How Supplied:

16 how supplied/storage and handling atropine sulfate ophthalmic solution, usp 1% is supplied as an aseptically prepared, sterile solution for topical ophthalmic use supplied as a 0.4 ml fill in a translucent, low-density polyethylene, single-dose vial. one (1) strip of 5 single-dose vials is packaged into a foil pouch. ndc 24208-965-01 10 single-dose vials. 2 foil pouches each containing one strip of 5 single-dose vials. storage and handling: store at 20°c to 25°c (68°f to 77°f). store single-dose vials in the foil pouches. opened vials cannot be resealed and should be discarded immediately after use.

Information for Patients:

17 patient counseling information • advise patients that drops will sting upon instillation that they may experience blurry vision and sensitivity to light and should protect their eyes in bright illumination during dilation. these effects may last up to a couple weeks. • advise patients to keep the single-dose vials in the foil pouches until ready to use. the solution from one single-dose vial is to be used immediately after opening to dose one or both eye(s) of a single patient. the single-dose vial, including any remaining contents, should be discarded immediately after administration [see dosage and administration (2) ] . • advise patients not to touch the tip of the single-dose vial to their eye or to any surface, in order to avoid eye injury or contamination of the solution. distributed by: bausch & lomb americas inc. bridgewater, nj 08807 usa © 2022 bausch & lomb incorporated or its affiliates 9775700

Package Label Principal Display Panel:

Package/label display panel ndc 24208-965-01 atropine sulfate ophthalmic solution, usp 1% sterile for topical ophthalmic use not for injection rx only 10 x 0.4 ml single-dose vials bausch + lomb 9769500 carton


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