Gentamicin Sulfate

Remedyrepack Inc.
Human Prescription Drug
NDC 70518-1323

Gentamicin Sulfate is a human prescription drug labeled by 'Remedyrepack Inc.'. National Drug Code (NDC) number for Gentamicin Sulfate is 70518-1323. This drug is available in dosage form of Solution. The names of the active, medicinal ingredients in Gentamicin Sulfate drug includes Gentamicin Sulfate - 3 mg/mL . The currest status of Gentamicin Sulfate drug is Active.

Drug Information:

Drug NDC:	70518-1323
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:	Gentamicin 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:	Gentamicin Sulfate
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Remedyrepack Inc.
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:	GENTAMICIN SULFATE - 3 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:	ANDA
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:	26 Jul, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	14 Jan, 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:	ANDA062196
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:	REMEDYREPACK INC.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:	310467
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.
UNII:	8X7386QRLV
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:	Aminoglycoside Antibacterial [EPC] Aminoglycosides [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
70518-1323-0	5 mL in 1 BOTTLE, PLASTIC (70518-1323-0)	26 Jul, 2018	N/A	No
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.

Other medicines with the same generic name

Gentamicin

Gentamicin Sulfate In Sodium Chloride

Gentamicin Sulfate

Injection, Solution
Baxter Healthcare Corporation
NDC: 0338-0503

Gentamicin Sulfate

Solution/ Drops
NuCare Pharmaceuticals, Inc.
NDC: 66267-971

Gentamicin Sulfate

Solution/ Drops
Bausch & Lomb Incorporated
NDC: 24208-580

Gentamicin Sulfate

Cream
Padagis Israel Pharmaceuticals Ltd
NDC: 45802-056

Product Elements:

Gentamicin sulfate gentamicin sulfate benzalkonium chloride sodium chloride sodium phosphate tyloxapol sodium hydroxide hydrochloric acid water gentamicin sulfate gentamicin

Indications and Usage:

Indications and usage gentamicin sulfate ophthalmic solution is indicated in the topical treatment of ocular bacterial infections, including conjunctivitis, keratitis, keratoconjunctivitis, corneal ulcers, blepharitis, blepharoconjunctivitis, acute meibomianitis, and dacryocystitis caused by susceptible strains of the following microorganisms: staphylococcus aureus, staphylococcus epidermidis, streptococcus pyogenes, streptococcus pneumoniae, enterobacter aerogenes, escherichia coli, haemophilus influenzae, klebsiella pneumoniae, neisseria gonorrhoeae, pseudomonas aeruginosa, and serratia marcescens.

Warnings:

Warnings not for injection into the eye. gentamicin sulfate ophthalmic solution is not for injection. it should never be injected subconjunctivally, nor should it be directly introduced into the anterior chamber of the eye.

Dosage and Administration:

Dosage and administration instill one or two drops into the affected eye(s) every four hours. in severe infections, dosage may be increased to as much as two drops once every hour.

Contraindications:

Contraindications gentamicin sulfate ophthalmic solution is contraindicated in patients with known hypersensitivity to any of the components.

Adverse Reactions:

Adverse reactions bacterial and fungal corneal ulcers have developed during treatment with gentamicin ophthalmic preparations. the most frequently reported adverse reactions are ocular burning and irritation upon drug instillation, non-specific conjunctivitis, conjunctival epithelial defects, and conjunctival hyperemia. other adverse reactions which have occurred rarely are allergic reactions, thrombocytopenic purpura, and hallucinations. to report suspected adverse reactions, contact sandoz inc. at 1-800-525-8747 or fda at 1-800-fda-1088 or www.fda.gov/medwatch.

Use in Pregnancy:

Pregnancy pregnancy category c. gentamicin has been shown to depress body weights, kidney weights, and median glomerular counts in newborn rats when administered systemically to pregnant rats in daily doses approximately 500 times the maximum recommended ophthalmic human dose. there are no adequate and well-controlled studies in pregnant women. gentamicin should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Pediatric Use:

Pediatric use safety and effectiveness in neonates have not been established.

Description:

Description gentamicin sulfate is a water-soluble antibiotic of the aminoglycoside group. gentamicin sulfate ophthalmic solution is a sterile, aqueous solution buffered to approximately ph 7 for ophthalmic use. gentamicin is obtained from cultures of micromonospora purpurea . it is a mixture of the sulfate salts of gentamicin c 1 , c 2 , and c 1a . all three components appear to have similar antimicrobial activities. gentamicin sulfate occurs as white powder and is soluble in water and insoluble in alcohol. the structure is as follows: established name: gentamicin sulfate chemical name: 0-3-deoxy-4-c-methyl-3-(methylamino)-Î²-l-arabinopyranosyl-(1â6)-0-[2,6-diamino-2,3,4,6-tetradeoxy-Î±-d-erythro-hexopyranosyl-(1â4)]-2-deoxy-d-streptamine. ingredients: each ml contains: active: gentamicin sulfate usp (equivalent to 3 mg gentamicin). preservative: benzalkonium chloride 0.1 mg (0.01%). inactives: sodium chloride, dried sodium phosphate, tyloxapol, sodium hydroxide and/or hydrochloric acid (to adjust ph) and purified water. chemicalstructure

Clinical Pharmacology:

Clinical pharmacology microbiology: gentamicin sulfate is active in vitro against many strains of the following microorganisms: staphylococcus aureus, staphylococcus epidermidis, streptococcus pyogenes, streptococcus pneumoniae, enterobacter aerogenes, escherichia coli, haemophilus influenzae, klebsiella pneumoniae, neisseria gonorrhoeae, pseudomonas aeruginosa, and serratia marcescens.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility there are no published carcinogenicity or impairment of fertility studies on gentamicin. aminoglycoside antibiotics have been found to be non-mutagenic.

How Supplied:

How supplied gentamicin sulfate ophthalmic solution: 5 ml in plastic dispenser. ndc: 70518-1323-00 packaging: 5 ml in 1 bottle plastic type 0 storage protect from light and store away from heat. store at controlled room temperature 15Â° to 25Â°c (59Â° to 77Â°f). repackaged and distributed by: remedy repack, inc. 625 kolter dr. suite #4 indiana, pa 1-724-465-8762

Information for Patients:

Information for patients to avoid contamination, do not touch tip of container to the eye, eyelid, or any surface. repackaged by / distributed by: remedyrepack inc. 625 kolter drive, indiana, pa 15701 (724) 465-8762

Package Label Principal Display Panel:

Drug: gentamicin sulfate generic: gentamicin sulfate dosage: solution adminstration: ophthalmic ndc: 70518-1323-0 packaging: 5 ml in 1 bottle, plastic active ingredient(s): gentamicin sulfate 3mg in 1ml inactive ingredient(s): benzalkonium chloride sodium chloride sodium phosphate tyloxapol sodium hydroxide hydrochloric acid water mm1

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.