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Drug Catalog - Product Detail

DICLOFENAC SODIUM GEL 3% 100GM

NDC Mfr Size Str Form
68462-0355-94 GLENMARK PHARMACEUTICALS 100 3% GEL
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PACKAGE FILES

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Generic Name
DICLOFENAC SODIUM
Substance Name
DICLOFENAC SODIUM
Product Type
HUMAN PRESCRIPTION DRUG
Route
TOPICAL
Application Number
ANDA208301
Description
DESCRIPTION Diclofenac Sodium Gel, 3%, contains the active ingredient, diclofenac sodium, in a clear, transparent, colorless to slightly yellow gel base. Diclofenac sodium is a white to off white, hygroscopic crystalline powder, and melts at about 284°C. It is freely soluble in methanol, soluble in ethanol, sparingly soluble in water, and practically insoluble in chloroform and ether. The chemical name for diclofenac sodium is: Sodium [ o -(2,6-dichloranilino) phenyl] acetate Diclofenac sodium has a molecular weight of 318.13. The CAS number is CAS-15307-79-6. The structural formula is represented below: Diclofenac sodium gel, 3% also contains benzyl alcohol, sodium hyaluronate, polyethylene glycol monomethyl ether, and purified water. 1 g of Diclofenac Sodium Gel, 3% contains 30 mg of the active substance, diclofenac sodium. structure
How Supplied
HOW SUPPLIED Each gram of Diclofenac Sodium Gel, 3% contains 30 mg of diclofenac sodium. Diclofenac Sodium Gel, 3% is available as follows: NDC 76420-132-01 100 g tube (relabeled from NDC 68462-355-94) Storage: Store at 20° to 25°C (68° to 77°F); [See USP Controlled Room Temperature]. Protect from heat. Avoid freezing. † Voltaren® is a registered trademark of Novartis. Relabeled by: Enovachem PHARMACEUTICALS Torrance, CA 90501
Indications & Usage
INDICATIONS AND USAGE Diclofenac sodium gel is indicated for the topical treatment of actinic keratoses (AK). Sun avoidance is indicated during therapy.
Dosage and Administration
DOSAGE AND ADMINISTRATION Diclofenac Sodium Gel, 3% is applied to lesion areas twice daily. It is to be smoothed onto the affected skin gently. The amount needed depends upon the size of the lesion site. Assure that enough diclofenac sodium gel is applied to adequately cover each lesion. Normally 0.5 g of gel is used on each 5 cm x 5 cm lesion site. The recommended duration of therapy is from 60 days to 90 days. Complete healing of the lesion(s) or optimal therapeutic effect may not be evident for up to 30 days following cessation of therapy. Lesions that do not respond to therapy should be carefully re-evaluated and management reconsidered.