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Fluticasone Propionate - 0713-0631-31 - (Fluticasone Propionate)

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Drug Information of Fluticasone Propionate

Product NDC: 0713-0631
Proprietary Name: Fluticasone Propionate
Non Proprietary Name: Fluticasone Propionate
Active Ingredient(s): .5    mg/g & nbsp;   Fluticasone Propionate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Fluticasone Propionate

Product NDC: 0713-0631
Labeler Name: G & W LABORATORIES, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077055
Marketing Category: ANDA
Start Marketing Date: 20060630

Package Information of Fluticasone Propionate

Package NDC: 0713-0631-31
Package Description: 30 g in 1 TUBE (0713-0631-31)

NDC Information of Fluticasone Propionate

NDC Code 0713-0631-31
Proprietary Name Fluticasone Propionate
Package Description 30 g in 1 TUBE (0713-0631-31)
Product NDC 0713-0631
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluticasone Propionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20060630
Marketing Category Name ANDA
Labeler Name G & W LABORATORIES, INC.
Substance Name FLUTICASONE PROPIONATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Fluticasone Propionate


General Information