Clindamycin Phosphate


Amneal Pharmaceuticals Ny Llc
Human Prescription Drug
NDC 69238-2031
Clindamycin Phosphate is a human prescription drug labeled by 'Amneal Pharmaceuticals Ny Llc'. National Drug Code (NDC) number for Clindamycin Phosphate is 69238-2031. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in Clindamycin Phosphate drug includes Clindamycin Phosphate - 1 g/10mL . The currest status of Clindamycin Phosphate drug is Active.

Drug Information:

Drug NDC: 69238-2031
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: Clindamycin Phosphate
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: Clindamycin Phosphate
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Amneal Pharmaceuticals Ny Llc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Gel
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:CLINDAMYCIN PHOSPHATE - 1 g/10mL
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: 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: 08 Aug, 2022
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 18 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: ANDA214668
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:Amneal Pharmaceuticals NY LLC
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UPC:0369238203172
UPC stands for Universal Product Code.
UNII:EH6D7113I8
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:Decreased Sebaceous Gland Activity [PE]
Lincosamide Antibacterial [EPC]
Lincosamides [CS]
Neuromuscular Blockade [PE]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
69238-2031-71 BOTTLE in 1 CARTON (69238-2031-7) / 75 mL in 1 BOTTLE08 Aug, 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:

Clindamycin phosphate clindamycin phosphate clindamycin phosphate clindamycin propylene glycol polyethylene glycol 400 methylparaben carbomer homopolymer type a sodium hydroxide water clear, colorless

Drug Interactions:

Drug interactions clindamycin has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. therefore, it should be used with caution in patients receiving such agents.

Indications and Usage:

Indications and usage clindamycin phosphate gel, 1% is indicated for topical application in the treatment of acne vulgaris. in view of the potential for diarrhea, bloody diarrhea and pseudomembranous colitis, the physician should consider whether other agents are more appropriate (see contraindications , warnings , and adverse reactions ).

Warnings:

Warnings orally and parenterally administered clindamycin has been associated with severe colitis, which may result in patient death. use of the topical formulation of clindamycin results in absorption of the antibiotic from the skin surface. diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported with the use of topical and systemic clindamycin. studies indicate a toxin(s) produced by clostridia is one primary cause of antibiotic-associated colitis. the colitis is usually characterized by severe persistent diarrhea and severe abdominal cramps and may be associated with the passage of blood and mucus. endoscopic examination may reveal pseudomembranous colitis. stool culture for clostridium difficile and stool assay for c. difficile toxin may be helpful diagnostically. when significant diarrhea occurs, the drug should be discontinued. large bowel endoscopy should be considered to establish a definitive diagnosis in cases of severe diarrhea. antiper
istaltic agents, such as opiates and diphenoxylate with atropine, may prolong and/or worsen the condition. diarrhea, colitis, and pseudomembranous colitis have been observed to begin up to several weeks following cessation of oral and parenteral therapy with clindamycin.

General Precautions:

General clindamycin phosphate gel should be prescribed with caution in atopic individuals.

Dosage and Administration:

Dosage and administration apply a thin film of clindamycin phosphate gel, 1% once daily to the skin where acne lesions appear. use enough to cover the entire affected area lightly. keep container tightly closed.

Contraindications:

Contraindications clindamycin phosphate gel is contraindicated in individuals with a history of hypersensitivity to preparations containing clindamycin or lincomycin, a history of regional enteritis or ulcerative colitis, or a history of antibiotic-associated colitis.

Adverse Reactions:

Adverse reactions in the one well-controlled clinical study comparing clindamycin phosphate gel and its vehicle, the incidence of skin and appendages adverse events occurring in ≥1% of the patients in either group is presented below: number (%) of patients body system/adverse event clindamycin phosphate gel qd (n=168) vehicle gel qd (n=84) skin and appendages disorders dermatitis 0 (0.0) 1 (1.2) dermatitis contact 0 (0.0) 1 (1.2) dermatitis fungal 0 (0.0) 1 (1.2) folliculitis 0 (0.0) 1 (1.2) photosensitivity reaction 0 (0.0) 1 (1.2) pruritus 1 (0.6) 1 (1.2) rash erythematous 0 (0.0) 0 (0.0) skin dry 0 (0.0) 0 (0.0) peeling 1 (0.6) 0 (0.0) orally and parenterally administered clindamycin has been associated with severe colitis, which may end fatally. cases of diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported as adverse reactions in patients treated with oral and parenteral formulations of clindamycin and rarely with topical clindamycin (
see warnings ). abdominal pain and gastrointestinal disturbances, as well as gram-negative folliculitis, have also been reported in association with the use of topical formulations of clindamycin. to report suspected adverse reactions, contact amneal pharmaceuticals at 1-877-835-5472 or fda at 1-800-fda-1088 or www.fda.gov/medwatch.

Adverse Reactions Table:

Number (%) of Patients
Body System/Adverse EventClindamycin Phosphate Gel QD (N=168)Vehicle Gel QD (N=84)
Skin and appendages disorders
Dermatitis0 (0.0)1 (1.2)
Dermatitis contact0 (0.0)1 (1.2)
Dermatitis fungal0 (0.0)1 (1.2)
Folliculitis0 (0.0)1 (1.2)
Photosensitivity reaction0 (0.0)1 (1.2)
Pruritus1 (0.6)1 (1.2)
Rash erythematous0 (0.0)0 (0.0)
Skin dry0 (0.0)0 (0.0)
Peeling1 (0.6)0 (0.0)

Drug Interactions:

Drug interactions clindamycin has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. therefore, it should be used with caution in patients receiving such agents.

Use in Pregnancy:

Pregnancy: teratogenic effects reproduction studies have been performed in rats and mice using subcutaneous and oral doses of clindamycin phosphate, clindamycin hydrochloride and clindamycin palmitate hydrochloride. these studies revealed no evidence of fetal harm. the highest dose used in the rat and mouse teratogenicity studies was equivalent to a clindamycin phosphate dose of 432 mg/kg. for a rat, this dose is 84 fold higher, and for a mouse 42 fold higher, than the anticipated human dose of clindamycin phosphate from clindamycin phosphate gel based on a mg/m 2 comparison. there are, however, no adequate and well-controlled studies in pregnant women. because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

Pediatric Use:

Pediatric use safety and effectiveness in children under the age of 12 have not been established.

Geriatric Use:

Geriatric use the clinical study with clindamycin phosphate gel did not include sufficient numbers of patients aged 65 and over to determine if they respond differently than younger patients.

Overdosage:

Overdosage topically applied clindamycin phosphate gel may be absorbed in sufficient amounts to produce systemic effects (see warnings ).

Description:

Description clindamycin phosphate gel usp, 1%, a topical antibiotic, contains clindamycin phosphate, usp, at a concentration equivalent to 10 mg clindamycin per gram in a gel vehicle consisting of propylene glycol, polyethylene glycol 400, methylparaben, carbomer homopolymer type a, sodium hydroxide and purified water. chemically, clindamycin phosphate, usp is a water-soluble ester of the semi-synthetic antibiotic produced by a 7 (s)-chloro-substitution of the 7 (r)-hydroxyl group of the parent antibiotic, lincomycin, and has the structural formula represented below: the chemical name for clindamycin phosphate, usp is methyl 7-chloro-6,7,8-trideoxy-6-(1-methyl- trans -4-propyl-l-2-pyrrolidinecarboxamido)-1-thio-l- threo -α-d- galacto -octopyranoside 2-(dihydrogen phosphate). structural formula

Clinical Pharmacology:

Clinical pharmacology pharmacokinetics in an open label, parallel group study of 24 patients with acne vulgaris, once-daily topical administration of approximately 3 to 12 grams/day of clindamycin phosphate gel for five days resulted in peak plasma clindamycin concentrations that were less than 5.5 ng/ml. following multiple applications of clindamycin phosphate gel less than 0.04% of the total dose was excreted in the urine. microbiology although clindamycin phosphate is inactive in vitro , rapid in vitro hydrolysis converts this compound to clindamycin which has antibacterial activity. clindamycin inhibits bacteria protein synthesis at the ribosomal level by binding to the 50s ribosomal subunit and affecting the process of peptide chain initiation. in vitro studies indicated that clindamycin inhibited all tested propionibacterium acnes cultures at a minimum inhibitory concentration (mic) of 0.4 mcg/ml. cross-resistance has been demonstrated between clindamycin and erythromycin.

Pharmacokinetics:

Pharmacokinetics in an open label, parallel group study of 24 patients with acne vulgaris, once-daily topical administration of approximately 3 to 12 grams/day of clindamycin phosphate gel for five days resulted in peak plasma clindamycin concentrations that were less than 5.5 ng/ml. following multiple applications of clindamycin phosphate gel less than 0.04% of the total dose was excreted in the urine. microbiology although clindamycin phosphate is inactive in vitro , rapid in vitro hydrolysis converts this compound to clindamycin which has antibacterial activity. clindamycin inhibits bacteria protein synthesis at the ribosomal level by binding to the 50s ribosomal subunit and affecting the process of peptide chain initiation. in vitro studies indicated that clindamycin inhibited all tested propionibacterium acnes cultures at a minimum inhibitory concentration (mic) of 0.4 mcg/ml. cross-resistance has been demonstrated between clindamycin and erythromycin.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility the carcinogenicity of a 1% clindamycin phosphate gel similar to clindamycin phosphate gel was evaluated by daily application to mice for two years. the daily doses used in this study were approximately 3 and 15 times higher than the human dose of clindamycin phosphate from 5 milliliters of clindamycin phosphate gel, assuming complete absorption and based on a body surface area comparison. no significant increase in tumors was noted in the treated animals. a 1% clindamycin phosphate gel similar to clindamycin phosphate gel caused a statistically significant shortening of the median time to tumor onset in a study in hairless mice in which tumors were induced by exposure to simulated sunlight. genotoxicity tests performed included a rat micronucleus test and an ames salmonella reversion test. both tests were negative. reproduction studies in rats using oral doses of clindamycin hydrochloride and clindamycin palmitate hydrochloride have
revealed no evidence of impaired fertility.

Clinical Studies:

Clinical studies in one 12-week, multicenter, randomized, evaluator-blind, vehicle-controlled, parallel comparison clinical trial in which patients used clindamycin phosphate gel, 1% once daily or the vehicle gel once daily, in the treatment of acne vulgaris of mild to moderate severity, clindamycin phosphate gel applied once daily was more effective than the vehicle applied once daily. the mean percent reductions in lesion counts at the end of treatment in this study are shown in the following table: lesions clindamycin phosphate gel qd n=162 vehicle gel qd n=82 inflammatory 51% 40% * noninflammatory 25% 12% * total 38% 27% * *p< 0.05 there was a trend in the investigator’s global assessment of the results which favored clindamycin phosphate gel qd over the vehicle qd. in a contact sensitization study, four of the 200 subjects appeared to develop suggestive evidence of allergic contact sensitization to clindamycin phosphate gel. there was no signal for contact sensitization in th
e clinical trials under normal use conditions.

How Supplied:

How supplied clindamycin phosphate gel usp, 1% containing clindamycin phosphate, usp equivalent to 10 mg clindamycin per gram, is available in the following size: 75 ml bottle - ndc 69238-2031-7 store at 20° to 25°c (68° to 77°f); excursions permitted between 15° to 30°c (59° to 86°f) [see usp controlled room temperature]. do not store in direct sunlight. caution federal law prohibits dispensing without prescription. distributed by: amneal pharmaceuticals llc bridgewater, nj 08807 rev. 04-2021-00

Package Label Principal Display Panel:

Principal display panel label carton


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