Cortifoam - 68220-140-15 - (hydrocortisone acetate)

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Drug Information of Cortifoam

Product NDC: 68220-140
Proprietary Name: Cortifoam
Non Proprietary Name: hydrocortisone acetate
Active Ingredient(s): 1500    mg/15g & nbsp;   hydrocortisone acetate
Administration Route(s): RECTAL
Dosage Form(s): AEROSOL, FOAM
Coding System: National Drug Codes(NDC)

Labeler Information of Cortifoam

Product NDC: 68220-140
Labeler Name: Alaven Pharmaceutical LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017351
Marketing Category: NDA
Start Marketing Date: 19820212

Package Information of Cortifoam

Package NDC: 68220-140-15
Package Description: 1 CONTAINER in 1 CARTON (68220-140-15) > 15 g in 1 CONTAINER

NDC Information of Cortifoam

NDC Code 68220-140-15
Proprietary Name Cortifoam
Package Description 1 CONTAINER in 1 CARTON (68220-140-15) > 15 g in 1 CONTAINER
Product NDC 68220-140
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocortisone acetate
Dosage Form Name AEROSOL, FOAM
Route Name RECTAL
Start Marketing Date 19820212
Marketing Category Name NDA
Labeler Name Alaven Pharmaceutical LLC
Substance Name HYDROCORTISONE ACETATE
Strength Number 1500
Strength Unit mg/15g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Cortifoam


General Information