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Hydrocortisone - 47682-211-12 - (Hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 47682-211
Proprietary Name: Hydrocortisone
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 10    mg/g & nbsp;   Hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 47682-211
Labeler Name: Unifirst First Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130415

Package Information of Hydrocortisone

Package NDC: 47682-211-12
Package Description: 10 POUCH in 1 BOX (47682-211-12) > .9 g in 1 POUCH (47682-211-99)

NDC Information of Hydrocortisone

NDC Code 47682-211-12
Proprietary Name Hydrocortisone
Package Description 10 POUCH in 1 BOX (47682-211-12) > .9 g in 1 POUCH (47682-211-99)
Product NDC 47682-211
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130415
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Unifirst First Aid Corporation
Substance Name HYDROCORTISONE
Strength Number 10
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Hydrocortisone


General Information