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Diphenhydramine HCl - 62211-048-99 - (Diphenhydramine HCl)

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Drug Information of Diphenhydramine HCl

Product NDC: 62211-048
Proprietary Name: Diphenhydramine HCl
Non Proprietary Name: Diphenhydramine HCl
Active Ingredient(s): 25    mg/1 & nbsp;   Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Diphenhydramine HCl

Product NDC: 62211-048
Labeler Name: A&Z Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20030310

Package Information of Diphenhydramine HCl

Package NDC: 62211-048-99
Package Description: 69767 TABLET, COATED in 1 CARTON (62211-048-99)

NDC Information of Diphenhydramine HCl

NDC Code 62211-048-99
Proprietary Name Diphenhydramine HCl
Package Description 69767 TABLET, COATED in 1 CARTON (62211-048-99)
Product NDC 62211-048
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine HCl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20030310
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name A&Z Pharmaceutical, Inc.
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Diphenhydramine HCl


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