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Pramoxine Hydrochloride - 54868-5865-0 - (pramoxine hydrochloride)

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Drug Information of Pramoxine Hydrochloride

Product NDC: 54868-5865
Proprietary Name: Pramoxine Hydrochloride
Non Proprietary Name: pramoxine hydrochloride
Active Ingredient(s): 150    mg/15g & nbsp;   pramoxine hydrochloride
Administration Route(s): RECTAL
Dosage Form(s): AEROSOL, FOAM
Coding System: National Drug Codes(NDC)

Labeler Information of Pramoxine Hydrochloride

Product NDC: 54868-5865
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part346
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080222

Package Information of Pramoxine Hydrochloride

Package NDC: 54868-5865-0
Package Description: 1 CONTAINER in 1 CARTON (54868-5865-0) > 15 g in 1 CONTAINER

NDC Information of Pramoxine Hydrochloride

NDC Code 54868-5865-0
Proprietary Name Pramoxine Hydrochloride
Package Description 1 CONTAINER in 1 CARTON (54868-5865-0) > 15 g in 1 CONTAINER
Product NDC 54868-5865
Product Type Name HUMAN OTC DRUG
Non Proprietary Name pramoxine hydrochloride
Dosage Form Name AEROSOL, FOAM
Route Name RECTAL
Start Marketing Date 20080222
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Physicians Total Care, Inc.
Substance Name PRAMOXINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/15g
Pharmaceutical Classes

Complete Information of Pramoxine Hydrochloride


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