Home > National Drug Code (NDC) > Hydrocortisone

Hydrocortisone - 0168-0020-16 - (Hydrocortisone)

Alphabetical Index


Drug Information of Hydrocortisone

Product NDC: 0168-0020
Proprietary Name: Hydrocortisone
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 10    mg/g & nbsp;   Hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 0168-0020
Labeler Name: E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080692
Marketing Category: ANDA
Start Marketing Date: 19750416

Package Information of Hydrocortisone

Package NDC: 0168-0020-16
Package Description: 453.6 g in 1 JAR (0168-0020-16)

NDC Information of Hydrocortisone

NDC Code 0168-0020-16
Proprietary Name Hydrocortisone
Package Description 453.6 g in 1 JAR (0168-0020-16)
Product NDC 0168-0020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19750416
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Substance Name HYDROCORTISONE
Strength Number 10
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone


General Information