Inveltys

Loteprednol Etabonate


Alcon Laboratories, Inc.
Human Prescription Drug
NDC 71571-121
Inveltys also known as Loteprednol Etabonate is a human prescription drug labeled by 'Alcon Laboratories, Inc.'. National Drug Code (NDC) number for Inveltys is 71571-121. This drug is available in dosage form of Suspension. The names of the active, medicinal ingredients in Inveltys drug includes Loteprednol Etabonate - 10 mg/mL . The currest status of Inveltys drug is Active.

Drug Information:

Drug NDC: 71571-121
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: Inveltys
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: Loteprednol Etabonate
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Alcon Laboratories, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Suspension
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:LOTEPREDNOL ETABONATE - 10 mg/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:TOPICAL
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: 22 Aug, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 21 Dec, 2025
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: NDA210565
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:ALCON LABORATORIES, INC.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:2055281
2055286
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:YEH1EZ96K6
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:Corticosteroid Hormone Receptor Agonists [MoA]
Corticosteroid [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
71571-121-202.8 mL in 1 BOTTLE, DROPPER (71571-121-20)22 Aug, 2018N/AYes
71571-121-281 BOTTLE, DROPPER in 1 CARTON (71571-121-28) / 2.8 mL in 1 BOTTLE, DROPPER22 Aug, 2018N/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:

Inveltys loteprednol etabonate loteprednol etabonate loteprednol glycerin trisodium citrate dihydrate sodium chloride edetate disodium citric acid monohydrate water

Indications and Usage:

1 indications and usage inveltys is a corticosteroid indicated for the treatment of post-operative inflammation and pain following ocular surgery. inveltys is a corticosteroid indicated for the treatment of post-operative inflammation and pain following ocular surgery. ( 1 )

Warnings and Cautions:

5 warnings and precautions intraocular pressure (iop) increase : prolonged use of corticosteroids may result in glaucoma with damage to the optic nerve, defects in visual acuity and fields of vision. if this product is used for 10 days or longer, iop should be monitored. ( 5.1 ) cataracts : use of corticosteroids may result in posterior subcapsular cataract formation. ( 5.2 ) delayed healing : use of steroids after cataract surgery may delay healing and increase the incidence of bleb formation. in those diseases causing thinning of the cornea or sclera, perforations have been known to occur with the use of topical steroids. the initial prescription and renewal of the medication order should be made by a physician only after examination of the patient with the aid of magnification such as slit lamp biomicroscopy and, where appropriate, fluorescein staining. ( 5.3 ) bacterial infections : prolonged use of corticosteroids may suppress the host response and thus increase the hazard of seco
ndary ocular infections. in acute purulent conditions, steroids may mask infection or enhance existing infection. ( 5.4 ) viral infections : use of a corticosteroid medication in the treatment of patients with a history of herpes simplex requires great caution. use of ocular steroids may prolong the course and may exacerbate the severity of many viral infections of the eye (including herpes simplex). ( 5.5 ) fungal infections : fungal infections of the cornea are particularly prone to develop coincidentally with long-term local steroid application. fungus invasion must be considered in any persistent corneal ulceration where a steroid has been used or is in use. ( 5.6 ) 5.1 intraocular pressure (iop) increase prolonged use of corticosteroids may result in glaucoma with damage to the optic nerve, as well as defects in visual acuity and fields of vision. steroids should be used with caution in the presence of glaucoma. if this product is used for 10 days or longer, intraocular pressure should be monitored. 5.2 cataracts use of corticosteroids may result in posterior subcapsular cataract formation. 5.3 delayed healing use of steroids after cataract surgery may delay healing and increase the incidence of bleb formation. in those diseases causing thinning of the cornea or sclera, perforations have been known to occur with the use of topical steroids. the initial prescription and renewal of the medication order should be made by a physician only after examination of the patient with the aid of magnification such as slit lamp biomicroscopy and, where appropriate, fluorescein staining. 5.4 bacterial infections prolonged use of corticosteroids may suppress the host response and thus increase the hazard of secondary ocular infections. in acute purulent conditions of the eye, steroids may mask infection or enhance existing infection. 5.5 viral infections use of corticosteroid medication in the treatment of patients with a history of herpes simplex requires great caution. use of ocular steroids may prolong the course and may exacerbate the severity of many viral infections of the eye (including herpes simplex). 5.6 fungal infections fungal infections of the cornea are particularly prone to develop coincidentally with long-term local steroid application. fungus invasion must be considered in any persistent corneal ulceration where a steroid has been used or is in use. fungal cultures should be taken when appropriate. 5.7 risk of contamination do not to allow the dropper tip to touch any surface, as this may contaminate the suspension. 5.8 contact lens wear the preservative in inveltys may be absorbed by soft contact lenses. contact lenses should be removed prior to instillation of inveltys and may be reinserted 15 minutes following administration.

Dosage and Administration:

2 dosage and administration shake for one to two seconds before using. ( 2 ) instill one to two drops of inveltys into the affected eye twice daily beginning the day after surgery and continuing throughout the first 2 weeks of the post-operative period. ( 2 ) 2.1 dosage information instill one to two drops of inveltys into the affected eye twice daily beginning the day after surgery and continuing throughout the first 2 weeks of the post-operative period. 2.2 administration instructions instruct patient to wash hands well before each use. shake for one to two seconds before using. if the patient is using other eye drops in addition to inveltys , advise the patient to wait at least 5 minutes between instillation of inveltys and other eye drops.

2.1 dosage information instill one to two drops of inveltys into the affected eye twice daily beginning the day after surgery and continuing throughout the first 2 weeks of the post-operative period.

2.2 administration instructions instruct patient to wash hands well before each use. shake for one to two seconds before using. if the patient is using other eye drops in addition to inveltys , advise the patient to wait at least 5 minutes between instillation of inveltys and other eye drops.

Dosage Forms and Strength:

3 dosage forms and strengths ophthalmic suspension containing 10 mg/ml of loteprednol etabonate. ophthalmic suspension containing 10 mg/ml of loteprednol etabonate. ( 3 )

Contraindications:

4 contraindications inveltys is contraindicated in most viral diseases of the cornea and conjunctiva including epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, and varicella, and also in mycobacterial infection of the eye and fungal diseases of ocular structures. inveltys is contraindicated in most viral diseases of the cornea and conjunctiva including epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, and varicella, and also in mycobacterial infection of the eye and fungal diseases of ocular structures. ( 4 )

Adverse Reactions:

6 adverse reactions adverse reactions associated with ophthalmic steroids include elevated intraocular pressure, which may be associated with infrequent optic nerve damage, visual acuity and field defects, posterior subcapsular cataract formation, delayed wound healing and secondary ocular infection from pathogens including herpes simplex, and perforation of the globe where there is thinning of the cornea or sclera. the most common adverse drug reactions were eye pain (1%) and posterior capsular opacification (1%). these reactions may have been the consequence of the surgical procedure. ( 6 ) to report suspected adverse reactions, contact kala pharmaceuticals, inc. at 1-833-287-kala (1-833-287-5252) or fda at 1-800-fda-1088 or www.fda.gov/medwatch . 6.1 clinical trials experience because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another dr
ug and may not reflect the rates observed in practice. the most common adverse drug reactions in the clinical trials with inveltys were eye pain and posterior capsular opacification, both reported in 1% of patients. these reactions may have been the consequence of the surgical procedure.

Use in Specific Population:

8 use in specific populations 8.1 pregnancy risk summary inveltys is not absorbed systemically following topical ophthalmic administration and maternal use is not expected to result in fetal exposure to the drug. 8.2 lactation risk summary inveltys is not absorbed systemically by the mother following topical ophthalmic administration, and breastfeeding is not expected to result in exposure of the child to inveltys . 8.3 pediatric use safety and effectiveness in pediatric patients have not been established. 8.4 geriatric use no overall differences in safety and effectiveness have been observed between elderly and younger patients.

Use in Pregnancy:

8.1 pregnancy risk summary inveltys is not absorbed systemically following topical ophthalmic administration and maternal use is not expected to result in fetal exposure to the drug.

Pediatric Use:

8.3 pediatric use safety and effectiveness in pediatric patients have not been established.

Geriatric Use:

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

Description:

11 description loteprednol etabonate is a corticosteroid. its chemical name is chloromethyl 17α-[(ethoxycarbonyl)oxy]-11β-hydroxy-3-oxoandrosta-1,4-diene-17β-carboxylate. its molecular formula is c 24 h 31 clo 7 and its chemical structure is: c 24 h 31 clo 7 mol. wt. 467.0 inveltys (loteprednol etabonate ophthalmic suspension) 1% contains a sterile, topical anti-inflammatory corticosteroid for ophthalmic use. each ml contains: active: loteprednol etabonate 10 mg (1%) inactives: glycerin, sodium citrate dihydrate, poloxamer 407, sodium chloride, edetate disodium dihydrate, citric acid, and water for injection preservative: benzalkonium chloride 0.01% chemical structure

Clinical Pharmacology:

12 clinical pharmacology 12.1 mechanism of action corticosteroids inhibit the inflammatory response to a variety of inciting agents and probably delay or slow healing. they inhibit the edema, fibrin deposition, capillary dilation, leukocyte migration, capillary proliferation, fibroblast proliferation, deposition of collagen, and scar formation associated with inflammation. while glucocorticoids are known to bind to and activate the glucocorticoid receptor, the molecular mechanisms involved in glucocorticoid/glucocorticoid receptor-dependent modulation of inflammation are not clearly established. however, corticosteroids are thought to inhibit prostaglandin production through several independent mechanisms. 12.3 pharmacokinetics loteprednol etabonate is lipid soluble and can penetrate into cells. loteprednol etabonate is synthesized through structural modifications of prednisolone-related compounds so that it will undergo a predictable transformation to an inactive metabolite. based upo
n in vivo and in vitro preclinical metabolism studies, loteprednol etabonate undergoes extensive metabolism to inactive carboxylic acid metabolites, pj-91 and pj-90. following twice-daily unilateral topical ocular dosing of inveltys for 14 days in healthy subjects, the plasma concentrations of loteprednol etabonate were below the limit of quantitation (1 ng/ml) at all timepoints.

Mechanism of Action:

12.1 mechanism of action corticosteroids inhibit the inflammatory response to a variety of inciting agents and probably delay or slow healing. they inhibit the edema, fibrin deposition, capillary dilation, leukocyte migration, capillary proliferation, fibroblast proliferation, deposition of collagen, and scar formation associated with inflammation. while glucocorticoids are known to bind to and activate the glucocorticoid receptor, the molecular mechanisms involved in glucocorticoid/glucocorticoid receptor-dependent modulation of inflammation are not clearly established. however, corticosteroids are thought to inhibit prostaglandin production through several independent mechanisms.

Pharmacokinetics:

12.3 pharmacokinetics loteprednol etabonate is lipid soluble and can penetrate into cells. loteprednol etabonate is synthesized through structural modifications of prednisolone-related compounds so that it will undergo a predictable transformation to an inactive metabolite. based upon in vivo and in vitro preclinical metabolism studies, loteprednol etabonate undergoes extensive metabolism to inactive carboxylic acid metabolites, pj-91 and pj-90. following twice-daily unilateral topical ocular dosing of inveltys for 14 days in healthy subjects, the plasma concentrations of loteprednol etabonate were below the limit of quantitation (1 ng/ml) at all timepoints.

Nonclinical Toxicology:

13 nonclinical toxicology 13.1 carcinogenesis, mutagenesis, impairment of fertility long-term animal studies have not been conducted to evaluate the carcinogenic potential of loteprednol etabonate. loteprednol etabonate was not genotoxic in vitro in the ames test, the mouse lymphoma thymidine kinase (tk) assay, or in a chromosome aberration test in human lymphocytes, or in vivo in the single dose mouse micronucleus assay.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

13.1 carcinogenesis, mutagenesis, impairment of fertility long-term animal studies have not been conducted to evaluate the carcinogenic potential of loteprednol etabonate. loteprednol etabonate was not genotoxic in vitro in the ames test, the mouse lymphoma thymidine kinase (tk) assay, or in a chromosome aberration test in human lymphocytes, or in vivo in the single dose mouse micronucleus assay.

Clinical Studies:

14 clinical studies clinical efficacy was evaluated in 2 multi-centered, randomized, double-masked, placebo-controlled trials in which patients with an anterior cell grade greater than or equal to "2" (a cell count of 6 or higher using a slit-lamp biomicroscope) after cataract surgery were assigned to inveltys or placebo (vehicle) following surgery (nct # 02163824 and nct # 02793817). one to two drops of inveltys or vehicle was self-administered twice a day for 14 days, beginning the day after surgery. complete resolution of inflammation (a cell count of 0 maintained through day 15 without rescue medication) and complete resolution of pain (a patient-reported pain grade of 0 maintained through day 15 without rescue medication) was assessed 4, 8, and 15 days post-surgery. in the intent-to-treat analysis of both studies, a significant benefit was seen in the inveltys -treated group for complete resolution of ocular inflammation at days 8 and 15, and complete resolution of pain at days 4,
8, and 15, when compared with placebo. the consolidated clinical trial results are provided below. figure 1 consolidated clinical trial data: percent of patients with complete resolution of anterior chamber cells (cell count = 0) at days 8 and 15 * p-values < 0.01 for treatment comparisons figure 2 consolidated clinical trial data: percent of patients who were pain free at days 4, 8, and 15 * p-values < 0.01 for treatment comparisons figure 1 figure 2

How Supplied:

16 how supplied/storage and handling inveltys (loteprednol etabonate ophthalmic suspension) 1% is a sterile ophthalmic suspension. it is supplied in a white low-density polyethylene plastic dropper bottle with a controlled-drop linear low-density polyethylene tip, a pink high-density polyethylene cap, and a white low-density polyethylene tamper-evident overcap in the following size: 2.8 ml in a 5 ml bottle (ndc 71571-121-28) storage and handling do not use if tamper-evident overcap seal is not intact. the white tamper-evident overcap can be thrown away. retain the pink cap and keep the bottle tightly closed when not in use. store upright at 15°c to 25°c (59°f to 77°f). do not freeze.

Information for Patients:

17 patient counseling information administration instruct the patient to shake the bottle for one to two seconds before using. if the patient is using other eye drops in addition to inveltys , advise the patient to wait at least 5 minutes between instillation of inveltys and other eye drops. risk of contamination advise patients to wash their hands well before each use. advise patients not to allow the dropper tip to touch any surface, as this may contaminate the suspension. risk of secondary infection advise the patient to consult a physician if pain develops, or redness, itching, or inflammation becomes aggravated. contact lens wear advise patients that the preservative in inveltys may be absorbed by soft contact lenses. contact lenses should be removed prior to instillation of inveltys and may be reinserted after 15 minutes following administration.

Package Label Principal Display Panel:

Principal display panel - 2.8 ml bottle carton ndc 71571-121-28 rx only inveltys ® (loteprednol etabonate ophthalmic suspension) 1% sterile 2.8 ml kala ® pharmaceuticals principal display panel - 2.8 ml bottle carton


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