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Hydrocortisone - 0168-0146-30 - (Hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 0168-0146
Proprietary Name: Hydrocortisone
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 25    mg/g & nbsp;   Hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 0168-0146
Labeler Name: E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA081203
Marketing Category: ANDA
Start Marketing Date: 19930528

Package Information of Hydrocortisone

Package NDC: 0168-0146-30
Package Description: 29 g in 1 TUBE (0168-0146-30)

NDC Information of Hydrocortisone

NDC Code 0168-0146-30
Proprietary Name Hydrocortisone
Package Description 29 g in 1 TUBE (0168-0146-30)
Product NDC 0168-0146
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19930528
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Substance Name HYDROCORTISONE
Strength Number 25
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone


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