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Hydrocortisone Valerate - 21695-730-15 - (Hydrocortisone Valerate)

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Drug Information of Hydrocortisone Valerate

Product NDC: 21695-730
Proprietary Name: Hydrocortisone Valerate
Non Proprietary Name: Hydrocortisone Valerate
Active Ingredient(s): 2    mg/g & nbsp;   Hydrocortisone Valerate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone Valerate

Product NDC: 21695-730
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075042
Marketing Category: ANDA
Start Marketing Date: 19980825

Package Information of Hydrocortisone Valerate

Package NDC: 21695-730-15
Package Description: 15 g in 1 TUBE (21695-730-15)

NDC Information of Hydrocortisone Valerate

NDC Code 21695-730-15
Proprietary Name Hydrocortisone Valerate
Package Description 15 g in 1 TUBE (21695-730-15)
Product NDC 21695-730
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone Valerate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19980825
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name HYDROCORTISONE VALERATE
Strength Number 2
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone Valerate


General Information