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Hydrocortisone - 0472-0337-20 - (Hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 0472-0337
Proprietary Name: Hydrocortisone
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 25    mg/g & nbsp;   Hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 0472-0337
Labeler Name: Actavis Mid Atlantic LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089682
Marketing Category: ANDA
Start Marketing Date: 20020930

Package Information of Hydrocortisone

Package NDC: 0472-0337-20
Package Description: 1 TUBE in 1 CARTON (0472-0337-20) > 20 g in 1 TUBE

NDC Information of Hydrocortisone

NDC Code 0472-0337-20
Proprietary Name Hydrocortisone
Package Description 1 TUBE in 1 CARTON (0472-0337-20) > 20 g in 1 TUBE
Product NDC 0472-0337
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20020930
Marketing Category Name ANDA
Labeler Name Actavis Mid Atlantic LLC
Substance Name HYDROCORTISONE
Strength Number 25
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone


General Information