Apexicon E

Diflorasone Diacetate


Pharmaderm A Division Of Fougera Pharmaceuticals Inc.
Human Prescription Drug
NDC 10337-395
Apexicon E also known as Diflorasone Diacetate is a human prescription drug labeled by 'Pharmaderm A Division Of Fougera Pharmaceuticals Inc.'. National Drug Code (NDC) number for Apexicon E is 10337-395. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Apexicon E drug includes Diflorasone Diacetate - .5 mg/g . The currest status of Apexicon E drug is Active.

Drug Information:

Drug NDC: 10337-395
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: Apexicon E
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: Diflorasone Diacetate
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Pharmaderm A Division Of Fougera Pharmaceuticals Inc.
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:DIFLORASONE DIACETATE - .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: 20 Dec, 2002
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 28 Apr, 2023
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: ANDA076263
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: 22 Dec, 2025
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:PharmaDerm a division of Fougera Pharmaceuticals Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:966577
966820
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.
UPC:0310337395602
UPC stands for Universal Product Code.
UNII:7W2J09SCWX
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
10337-395-301 TUBE in 1 CARTON (10337-395-30) / 30 g in 1 TUBE20 Dec, 200228 Apr, 2023No
10337-395-601 TUBE in 1 CARTON (10337-395-60) / 60 g in 1 TUBE20 Dec, 200228 Apr, 2023No
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:

Apexicon e diflorasone diacetate diflorasone diacetate diflorasone stearyl alcohol cetyl alcohol sorbitan monostearate mineral oil water polysorbate 60 propylene glycol

Indications and Usage:

Indications and usage topical corticosteroids are indicated for relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses.

Warnings:

Warnings use of topical corticosteroids, including apexicon® e cream (diflorasone diacetate 0.05% [emollient]) may increase the risk of posterior subcapsular cataracts and glaucoma. cataracts have been reported in postmarketing experience with the use of topical diflorasone diacetate products. glaucoma, with possible damage to the optic nerve, and increased intraocular pressure have been reported in postmarketing experience with the use of topical dermal corticosteroids. avoid contact of apexicon® e cream (diflorasone diacetate 0.05% [emollient]) with eyes. advise patients to report any visual symptoms.

General Precautions:

General: systemic absorption of topical corticosteroids has produced reversible hypothalamic-pituitary-adrenal (hpa) axis suppression, manifestations of cushing's syndrome, hyperglycemia, and glucosuria in some patients. conditions which augment systemic absorption include the application of the more potent steroids, use over large surface areas, prolonged use, and the addition of occlusive dressings. therefore, patients receiving a large dose of a potent topical steroid applied to a large surface area or under an occlusive dressing should be evaluated periodically for evidence of hpa axis suppression by using the urinary free cortisol and acth stimulation tests. 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 steroid. recovery of hpa axis function is generally prompt and complete upon discontinuation of the drug. infrequently, signs and symptoms of steroid withdrawal may occur, req
uiring supplemental systemic corticosteroids. pediatric patients may absorb proportionally larger amounts of topical corticosteroids and thus be more susceptible to systemic toxicity (see precautions: pediatric use ). if irritation develops, topical corticosteroids should be discontinued and appropriate therapy instituted. in the presence of dermatological infections, the use of an appropriate antifungal or antibacterial agent should be instituted. if a favorable response does not occur promptly, the corticosteroid should be discontinued until the infection has been adequately controlled.

Dosage and Administration:

Dosage and administration apexicon ® e cream (diflorasone diacetate cream 0.05% [emollient]) should be applied to the affected areas as a thin film from one to three times daily depending on the severity or resistant nature of the condition. for topical use only. avoid contact with eyes. wash hands after each application. do not use with occlusive dressings, unless directed by a physician (see precautions ). if an infection develops, the use of occlusive dressings should be discontinued and appropriate antimicrobial therapy initiated.

Contraindications:

Contraindications topical steroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

Adverse Reactions:

Adverse reactions the following adverse reactions have been identified from clinical trials or postmarketing surveillance. because they are reported from a population from unknown size, it is not always possible to reliably estimate their frequency or establish a causal relationship to topical corticosteroids exposure. these adverse reactions may occur more frequently with the use of occlusive dressings or prolonged use of topical corticosteroids. skin and subcutaneous tissue disorders: burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae, and miliaria vision disorders : cataract, glaucoma, central serous chorioretinopathy

Use in Pregnancy:

Pregnancy : corticosteroids are generally teratogenic in laboratory animals when administered systemically at relatively low dosage levels. the more potent corticosteroids have been shown to be teratogenic after dermal application in laboratory animals. there are no adequate and well-controlled studies in pregnant women on teratogenic effects from topically applied corticosteroids. therefore, topical corticosteroids should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. drugs of this class should not be used extensively on pregnant patients, in large amounts, or for prolonged periods of time.

Pediatric Use:

Pediatric use: safety and effectiveness of apexicon® e cream (diflorasone diacetate cream) in pediatric patients have not been established. 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 when they are treated with topical corticosteroids. they are, therefore, also at greater risk of glucocorticosteroid insufficiency after withdrawal of treatment and of cushing's syndrome while on treatment. adverse effects including striae have been reported with inappropriate use of topical corticosteroids in pediatric patients. hpa axis suppression, cushing's syndrome, and intracranial hypertension have been reported in pediatric patients receiving topical corticosteroids. manifestations of adrenal suppression in pediatric patients include linear growth retardation, delayed weight gain, low plasma cortisol levels, and absence of response to acth stimulation. manifestations of intracranial hypertension includ
e bulging fontanelles, headaches, and bilateral papilledema. geriatric use: clinical studies of diflorasone diacetate topical formulations did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects.

Overdosage:

Overdosage topically applied corticosteroids can be absorbed in sufficient amounts to produce systemic effects (see precautions ).

Description:

Description each gram of apexicon ® e cream (diflorasone diacetate cream usp, 0.05% [emollient]) contains 0.5 mg diflorasone diacetate in a cream base for topical dermatological use. chemically, diflorasone diacetate is: 6α, 9-difluoro-11β, 17, 21-trihydroxy-16β-methylpregna-1, 4-diene-3,20-dione 17,21-diacetate. the structural formula is represented below: each gram of apexicon ® e cream (diflorasone diacetate cream usp, 0.05% [emollient]) contains: 0.5 mg diflorasone diacetate in a hydrophilic vanishing cream base of propylene glycol, stearyl alcohol, cetyl alcohol, sorbitan monostearate, polysorbate 60, mineral oil and purified water. structuralformula

Clinical Pharmacology:

Clinical pharmacology topical corticosteroids share anti-inflammatory, antipruritic and vasoconstrictive actions. the mechanism of anti-inflammatory activity of the topical corticosteroids is unclear. various laboratory methods, including vasoconstrictor assays, are used to compare and predict potencies and/or clinical efficacies of the topical corticosteroids. there is some evidence to suggest that a recognizable correlation exists between vasoconstrictor potency and therapeutic efficacy in man. pharmacokinetics: the extent of percutaneous absorption of topical corticosteroids is determined by many factors including the vehicle, the integrity of the epidermal barrier, and the use of occlusive dressings. topical corticosteroids can be absorbed from normal intact skin. inflammation and/or other disease processes in the skin increase percutaneous absorption. occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids. thus, occlusive dressings may be
a valuable therapeutic adjunct for treatment of resistant dermatoses (see dosage and administration ). once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways similar to systemically administered corticosteroids. corticosteroids are bound to plasma proteins in varying degrees. they are metabolized primarily in the liver and are then excreted by the kidneys. some of the topical corticosteroids and their metabolites are also excreted into the bile.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, and impairment of fertility: long-term animal studies have not been performed to evaluate the carcinogenic potential or the effect on fertility of topical corticosteroids. diflorasone diacetate was not mutagenic in a micronucleus test in rats at intraperitoneal doses up to 2400 mg/kg.

How Supplied:

How supplied apexicon ® e cream (diflorasone diacetate cream usp, 0.05% [emollient]) is available in the following size tubes: ndc 10337-395-30 30 gram tube ndc 10337-395-60 60 gram tube store at controlled room temperature, 20° to 25°c (68° to 77°f) [see usp]. pharmaderm ® a division of fougerapharmaceuticals inc. melville, new york 11747 usa 46228067b/46268153a r04/2020 #35

Information for Patients:

Information for the patient : 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. patients should be advised not to use this medication for any disorder other than for which it was prescribed. 3. contact your healthcare provider if you experience blurred vision or other visual disturbances (see warnings ). 4. the treated skin area should not be bandaged or otherwise covered or wrapped as to be occlusive unless directed by the physician (see precautions ) . 5. patients should report any signs of local adverse reactions especially under occlusive dressing. 6. parents of pediatric patients should be advised not to use tight-fitting diapers or plastic pants on an infant or child being treated in the diaper area, as these garments may constitute occlusive dressings.

Package Label Principal Display Panel:

Package label – principal display panel – 60 g label ndc 10337-395-60 pharmaderm ® apexicon ® e cream (diflorasone diacetate cream usp 0.05% [emollient]) for external use only not for ophthalmic use rx only 60 g container60gtube.jpg

Package label – principal display panel – 60 g carton ndc 10337-395-60 pharmaderm ® apexicon ® e cream (diflorasone diacetate cream usp 0.05% [emollient]) for external use only not for ophthalmic use rx only 60 g principaldisplaypanel60g carton


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