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Fluticasone Propionate - 0713-0632-15 - (Fluticasone Propionate)

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Drug Information of Fluticasone Propionate

Product NDC: 0713-0632
Proprietary Name: Fluticasone Propionate
Non Proprietary Name: Fluticasone Propionate
Active Ingredient(s): .05    mg/g & nbsp;   Fluticasone Propionate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Fluticasone Propionate

Product NDC: 0713-0632
Labeler Name: GW Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077168
Marketing Category: ANDA
Start Marketing Date: 20060531

Package Information of Fluticasone Propionate

Package NDC: 0713-0632-15
Package Description: 15 g in 1 TUBE (0713-0632-15)

NDC Information of Fluticasone Propionate

NDC Code 0713-0632-15
Proprietary Name Fluticasone Propionate
Package Description 15 g in 1 TUBE (0713-0632-15)
Product NDC 0713-0632
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluticasone Propionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20060531
Marketing Category Name ANDA
Labeler Name GW Laboratories, Inc
Substance Name FLUTICASONE PROPIONATE
Strength Number .05
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Fluticasone Propionate


General Information