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hydrocortisone - 37808-885-64 - (Hydrocortisone)

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Drug Information of hydrocortisone

Product NDC: 37808-885
Proprietary Name: hydrocortisone
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 1    g/100g & nbsp;   Hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of hydrocortisone

Product NDC: 37808-885
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20101002

Package Information of hydrocortisone

Package NDC: 37808-885-64
Package Description: 1 TUBE in 1 CARTON (37808-885-64) > 28 g in 1 TUBE

NDC Information of hydrocortisone

NDC Code 37808-885-64
Proprietary Name hydrocortisone
Package Description 1 TUBE in 1 CARTON (37808-885-64) > 28 g in 1 TUBE
Product NDC 37808-885
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20101002
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name H E B
Substance Name HYDROCORTISONE
Strength Number 1
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of hydrocortisone


General Information