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FLUTICASONE PROPIONATE - 0168-0434-04 - (fluticasone propionate)

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Drug Information of FLUTICASONE PROPIONATE

Product NDC: 0168-0434
Proprietary Name: FLUTICASONE PROPIONATE
Non Proprietary Name: fluticasone propionate
Active Ingredient(s): .5    mg/mL & nbsp;   fluticasone propionate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of FLUTICASONE PROPIONATE

Product NDC: 0168-0434
Labeler Name: E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021152
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20091005

Package Information of FLUTICASONE PROPIONATE

Package NDC: 0168-0434-04
Package Description: 1 BOTTLE in 1 CARTON (0168-0434-04) > 120 mL in 1 BOTTLE

NDC Information of FLUTICASONE PROPIONATE

NDC Code 0168-0434-04
Proprietary Name FLUTICASONE PROPIONATE
Package Description 1 BOTTLE in 1 CARTON (0168-0434-04) > 120 mL in 1 BOTTLE
Product NDC 0168-0434
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluticasone propionate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20091005
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Substance Name FLUTICASONE PROPIONATE
Strength Number .5
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of FLUTICASONE PROPIONATE


General Information