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HYDROCORTISONE - 0168-0016-31 - (HYDROCORTISONE)

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Drug Information of HYDROCORTISONE

Product NDC: 0168-0016
Proprietary Name: HYDROCORTISONE
Non Proprietary Name: HYDROCORTISONE
Active Ingredient(s): 5    mg/g & nbsp;   HYDROCORTISONE
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of HYDROCORTISONE

Product NDC: 0168-0016
Labeler Name: E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19810101

Package Information of HYDROCORTISONE

Package NDC: 0168-0016-31
Package Description: 1 TUBE in 1 CARTON (0168-0016-31) > 28 g in 1 TUBE

NDC Information of HYDROCORTISONE

NDC Code 0168-0016-31
Proprietary Name HYDROCORTISONE
Package Description 1 TUBE in 1 CARTON (0168-0016-31) > 28 g in 1 TUBE
Product NDC 0168-0016
Product Type Name HUMAN OTC DRUG
Non Proprietary Name HYDROCORTISONE
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19810101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Substance Name HYDROCORTISONE
Strength Number 5
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of HYDROCORTISONE


General Information