Alclometasone Dipropionate


Glenmark Pharmaceuticals Inc., Usa
Human Prescription Drug
NDC 68462-300
Alclometasone Dipropionate is a human prescription drug labeled by 'Glenmark Pharmaceuticals Inc., Usa'. National Drug Code (NDC) number for Alclometasone Dipropionate is 68462-300. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Alclometasone Dipropionate drug includes Alclometasone Dipropionate - .5 mg/g . The currest status of Alclometasone Dipropionate drug is Active.

Drug Information:

Drug NDC: 68462-300
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: Alclometasone Dipropionate
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: Alclometasone Dipropionate
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Glenmark Pharmaceuticals Inc., Usa
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Cream
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:ALCLOMETASONE DIPROPIONATE - .5 mg/g
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: 23 Jun, 2009
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 26 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: ANDA079061
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:Glenmark Pharmaceuticals Inc., USA
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:855474
855480
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:S56PQL4N1V
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
68462-300-1715 g in 1 TUBE (68462-300-17)23 Jun, 2009N/ANo
68462-300-4745 g in 1 TUBE (68462-300-47)23 Jun, 2009N/ANo
68462-300-6560 g in 1 TUBE (68462-300-65)23 Jun, 2009N/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:

Alclometasone dipropionate alclometasone dipropionate alclometasone dipropionate alclometasone propylene glycol petrolatum cetostearyl alcohol sodium phosphate, monobasic, monohydrate chlorocresol phosphoric acid water glyceryl monostearate peg-100 stearate ceteth-20 alclometasone dipropionate alclometasone dipropionate alclometasone dipropionate alclometasone hexylene glycol white wax propylene glycol monopalmitostearate petrolatum

Indications and Usage:

Indications and usage alclometasone dipropionate cream and ointment are low to medium potency corticosteroids indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. alclometasone dipropionate cream and ointment may be used in pediatric patients 1 year of age or older, although the safety and efficacy of drug use for longer than 3 weeks have not been established (see precautions: pediatric use ). since the safety and efficacy of alclometasone dipropionate cream and ointment have not been established in pediatric patients below 1 year of age, their use in this age-group is not recommended.

General Precautions:

General systemic absorption of topical corticosteroids can produce reversible hypothalamic-pituitary-adrenal (hpa) axis suppression with the potential for glucocorticosteroid insufficiency after withdrawal of treatment. manifestations of cushing syndrome, hyperglycemia, and glucosuria can also be produced in some patients by systemic absorption of topical corticosteroids while on treatment. patients applying a topical steroid to a large surface area or to areas under occlusion should be evaluated periodically for evidence of hpa axis suppression. this may be done by using the acth stimulation, a.m. plasma cortisol, and urinary free cortisol tests. the effects of alclometasone dipropionate cream and ointment on the hpa axis have been evaluated. in one study, alclometasone dipropionate cream and ointment were applied to 30% of the body twice daily for 7 days, and occlusive dressings were used in selected patients either 12 hours or 24 hours daily. in another study, alclometasone dipropio
nate cream was applied to 80% of the body surface of normal subjects twice daily for 21 days with daily 12-hour periods of whole body occlusion. average plasma and urinary free cortisol levels and urinary levels of 17-hydroxysteroids were decreased (about 10%), suggesting suppression of the hpa axis under these conditions. plasma cortisol levels have also been demonstrated to decrease in pediatric patients treated twice daily for 3 weeks without occlusion. if hpa axis suppression is noted, an attempt should be made to withdraw the drug, to reduce the frequency of application, or to substitute a less potent corticosteroid. recovery of hpa axis function is generally prompt upon discontinuation of topical corticosteroids. infrequently, signs and symptoms of glucocorticosteroid insufficiency may occur, requiring supplemental systemic corticosteroids. for information on systemic supplementation, see prescribing information for those products. pediatric patients may be more susceptible to systemic toxicity from equivalent doses due to their larger skin surface area to body mass ratios (see precautions: pediatric use ). if irritation develops, alclometasone dipropionate cream or ointment should be discontinued and appropriate therapy instituted. allergic contact dermatitis with corticosteroids is usually diagnosed by observing a failure to heal rather than noting a clinical exacerbation, as with most topical products not containing corticosteroids. such an observation should be corroborated with appropriate diagnostic patch testing. if concomitant skin infections are present or develop, an appropriate antifungal or antibacterial agent should be used. if a favorable response does not occur promptly, use of alclometasone dipropionate cream or ointment should be discontinued until the infection has been adequately controlled. in a transgenic mouse study, chronic use of alclometasone dipropionate cream led to an increased number of animals with benign neoplasms of the skin at the treatment site (see precautions: carcinogenesis, mutagenesis, and impairment of fertility ). the clinical relevance of the findings in animal studies to humans is not clear.

Dosage and Administration:

Dosage and administration apply a thin film of alclometasone dipropionate cream or ointment to the affected skin areas 2 or 3 times daily; massage gently until the medication disappears. alclometasone dipropionate cream and ointment may be used in pediatric patients 1 year of age or older. safety and effectiveness of alclometasone dipropionate cream or ointment in pediatric patients for more than 3 weeks of use have not been established. use in pediatric patients under 1 year of age is not recommended. as with other corticosteroids, therapy should be discontinued when control is achieved. if no improvement is seen within 2 weeks, reassessment of diagnosis may be necessary. alclometasone dipropionate cream or ointment should not be used with occlusive dressings unless directed by a physician. alclometasone dipropionate cream or ointment should not be applied in the diaper area if the child still requires diapers or plastic pants as these garments may constitute occlusive dressing. geria
tric use : in studies where geriatric patients (65 years of age or older, see precautions ) have been treated with alclometasone dipropionate cream or ointment, safety did not differ from that in younger patients; therefore, no dosage adjustment is recommended.

Contraindications:

Contraindications alclometasone dipropionate cream and ointment are contraindicated in those patients with a history of hypersensitivity to any of the components in these preparations.

Adverse Reactions:

Adverse reactions the following local adverse reactions have been reported with alclometasone dipropionate cream in approximately 2% of patients: itching and burning, erythema, dryness, irritation, and papular rashes. the following local adverse reactions have been reported with alclometasone dipropionate ointment in approximately 1% of patients: itching, burning, and erythema. the following additional local adverse reactions have been reported infrequently with topical corticosteroids, but may occur more frequently with the use of occlusive dressings. these reactions are listed in approximate decreasing order of occurrence: folliculitis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, secondary infection, skin atrophy, striae, and miliaria.

Use in Pregnancy:

Pregnancy teratogenic effects corticosteroids have been shown to be teratogenic in laboratory animals when administered systemically at relatively low dosage levels. some corticosteroids have been shown to be teratogenic after dermal application in laboratory animals. there are no adequate and well-controlled studies in pregnant women. alclometasone dipropionate cream or ointment should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Pediatric Use:

Pediatric use alclometasone dipropionate cream and ointment may be used with caution in pediatric patients 1 year of age or older, although the safety and efficacy of drug use for longer than 3 weeks have not been established. use of alclometasone dipropionate cream and ointment is supported by results from adequate and well-controlled studies in pediatric patients with corticosteroid-responsive dermatoses. since the safety and efficacy of alclometasone dipropionate cream and ointment have not been established in pediatric patients below 1 year of age, its use in this age-group is not recommended. because of a higher ratio of skin surface area to body mass, pediatric patients are at a greater risk than adults of hpa axis suppression and cushing syndrome when they are treated with topical corticosteroids. they are therefore also at greater risk of adrenal insufficiency during and/or after withdrawal of treatment. adverse effects, including striae, have been reported with inappropriate u
se of topical corticosteroids in infants and children. pediatric patients applying alclometasone dipropionate cream or ointment to >20% of the body surface area are at higher risk for hpa axis suppression. hpa axis suppression, cushing syndrome, linear growth retardation, delayed weight gain, and intracranial hypertension have been reported in pediatric patients receiving topical corticosteroids. manifestations of adrenal suppression in pediatric patients include low plasma cortisol levels and absence of response to acth stimulation. manifestations of intracranial hypertension include bulging fontanelles, headaches, and bilateral papilledema. alclometasone dipropionate cream or ointment should not be used in the treatment of diaper dermatitis.

Geriatric Use:

Geriatric use a limited number of patients at or above 65 years of age have been treated with alclometasone dipropionate cream and ointment in us clinical trials. the number of patients is too small to permit separate analysis of efficacy and safety. no adverse events were reported with alclometasone dipropionate ointment in geriatric patients, and the single adverse reaction reported with alclometasone dipropionate cream in this population was similar to those reactions reported by younger patients. based on available data, no adjustment of dosage of alclometasone dipropionate cream and ointment in geriatric patients is warranted.

Overdosage:

Overdosage topically applied alclometasone dipropionate cream and ointment can be absorbed in sufficient amounts to produce systemic effects (see precautions ).

Description:

Description alclometasone dipropionate cream usp, 0.05% and alclometasone dipropionate ointment usp, 0.05% contain alclometasone dipropionate, usp (7α-chloro-11β,17,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione 17,21-dipropionate), a synthetic corticosteroid for topical dermatologic use. the corticosteroids constitute a class of primarily synthetic steroids used topically as anti-inflammatory and antipruritic agents. chemically, alclometasone dipropionate, usp is c 28 h 37 clo 7 . it has the following structural formula: alclometasone dipropionate, usp has the molecular weight of 521.04 g/mol. it is a white to almost white crystalline powder, sparingly soluble in alcohol, acetone, ethyl acetate and acetonitrile. each gram of alclometasone dipropionate cream usp contains 0.5 mg of alclometasone dipropionate, usp in a hydrophilic, emollient cream base of propylene glycol, white petrolatum, cetearyl alcohol, mono and di-glycerides, peg 100 stearate, ceteth-20, monobasic sodium phosphate, chlorocresol, phosphoric acid, and purified water. each gram of alclometasone dipropionate ointment usp contains 0.5 mg of alclometasone dipropionate, usp in an ointment base of hexylene glycol, white wax, propylene glycol monopalmitostearate, and white petrolatum. structure-formula

Clinical Pharmacology:

Clinical pharmacology like other topical corticosteroids, alclometasone dipropionate has anti-inflammatory, antipruritic, and vasoconstrictive properties. the mechanism of the anti-inflammatory activity of the topical steroids, in general, is unclear. however, corticosteroids are thought to act by the induction of phospholipase a 2 inhibitory proteins, collectively called lipocortins. it is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor, arachidonic acid. arachidonic acid is released from membrane phospholipids by phospholipase a 2 . pharmacokinetics the extent of percutaneous absorption of topical corticosteroids is determined by many factors, including the vehicle and the integrity of the epidermal barrier. occlusive dressings with hydrocortisone for up to 24 hours have not been demonstrated to increase penetration; however, occlusion of hydrocortis
one for 96 hours markedly enhances penetration. topical corticosteroids can be absorbed from normal intact skin. inflammation and/or other disease processes in the skin may increase percutaneous absorption. a study utilizing a radio labeled alclometasone dipropionate ointment formulation was performed to measure systemic absorption and excretion. results indicated that approximately 3% of the steroid was absorbed during 8 hours of contact with intact skin of normal volunteers. studies performed with alclometasone dipropionate cream and ointment indicate that these products are in the low to medium range of potency as compared with other topical corticosteroids.

Pharmacokinetics:

Pharmacokinetics the extent of percutaneous absorption of topical corticosteroids is determined by many factors, including the vehicle and the integrity of the epidermal barrier. occlusive dressings with hydrocortisone for up to 24 hours have not been demonstrated to increase penetration; however, occlusion of hydrocortisone for 96 hours markedly enhances penetration. topical corticosteroids can be absorbed from normal intact skin. inflammation and/or other disease processes in the skin may increase percutaneous absorption. a study utilizing a radio labeled alclometasone dipropionate ointment formulation was performed to measure systemic absorption and excretion. results indicated that approximately 3% of the steroid was absorbed during 8 hours of contact with intact skin of normal volunteers. studies performed with alclometasone dipropionate cream and ointment indicate that these products are in the low to medium range of potency as compared with other topical corticosteroids.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility systemic long-term animal studies have not been performed to evaluate the carcinogenic potential of alclometasone dipropionate. the effects of alclometasone dipropionate on mutagenesis or fertility have not been evaluated. in a 26-week dermal carcinogenicity study conducted in transgenic (tg.ac) mice, topical application once daily of both the vehicle cream and the 0.05% alclometasone dipropionate cream significantly increased the incidence of benign neoplasms of the skin in both sexes at the treatment site when compared to untreated controls. this suggests that the positive effect may be associated with the vehicle application. the clinical relevance of the findings in animals to humans is not clear.

How Supplied:

How supplied alclometasone dipropionate cream usp, 0.05% is supplied in: 15 gram tubes (ndc 68462-300-17) 45 gram tubes (ndc 68462-300-47) 60 gram tubes (ndc 68462-300-65) alclometasone dipropionate ointment usp, 0.05% is supplied in: 15 gram tubes (ndc 68462-299-17) 45 gram tubes (ndc 68462-299-47) 60 gram tubes (ndc 68462-299-65) store between 2°c and 30°c (36°f and 86°f).

Information for Patients:

Information for patients patients using topical corticosteroids should receive the following information and instructions: 1. this medication is to be used as directed by the physician. it is for external use only. avoid contact with the eyes. 2. this medication should not be used for any disorder other than that for which it was prescribed. 3. the treated skin area should not be bandaged, otherwise covered or wrapped so as to be occlusive, unless directed by the physician. 4. patients should report to their physician any signs of local adverse reactions. 5. parents of pediatric patients should be advised not to use alclometasone dipropionate cream or ointment in the treatment of diaper dermatitis. alclometasone dipropionate cream or ointment should not be applied in the diaper area as diapers or plastic pants may constitute occlusive dressing (see dosage and administration ). 6. this medication should not be used on the face, underarms, or groin areas unless directed by the physician.
7. as with other corticosteroids, therapy should be discontinued when control is achieved. if no improvement is seen within 2 weeks, contact the physician.

Package Label Principal Display Panel:

Principal display panel ndc 68462-300-47 alclometasone dipropionate cream usp, 0.05% for dermatologic use only – not for ophthalmic use. cream-carton

Ndc 68462-299-47 alclometasone dipropionate ointment usp, 0.05% for dermatologic use only – not for ophthalmic use ointment-carton


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