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Hydrocortisone - 0603-3900-32 - (hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 0603-3900
Proprietary Name: Hydrocortisone
Non Proprietary Name: hydrocortisone
Active Ingredient(s): 10    mg/1 & nbsp;   hydrocortisone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 0603-3900
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040761
Marketing Category: ANDA
Start Marketing Date: 20070716

Package Information of Hydrocortisone

Package NDC: 0603-3900-32
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0603-3900-32)

NDC Information of Hydrocortisone

NDC Code 0603-3900-32
Proprietary Name Hydrocortisone
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0603-3900-32)
Product NDC 0603-3900
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocortisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070716
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name HYDROCORTISONE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone


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