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diphenhydramine hydrochloride - 0185-0649-01 - (diphenhydramine hydrochloride)

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Drug Information of diphenhydramine hydrochloride

Product NDC: 0185-0649
Proprietary Name: diphenhydramine hydrochloride
Non Proprietary Name: diphenhydramine hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   diphenhydramine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of diphenhydramine hydrochloride

Product NDC: 0185-0649
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20000501

Package Information of diphenhydramine hydrochloride

Package NDC: 0185-0649-01
Package Description: 100 CAPSULE in 1 BOTTLE (0185-0649-01)

NDC Information of diphenhydramine hydrochloride

NDC Code 0185-0649-01
Proprietary Name diphenhydramine hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (0185-0649-01)
Product NDC 0185-0649
Product Type Name HUMAN OTC DRUG
Non Proprietary Name diphenhydramine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20000501
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Eon Labs, Inc.
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of diphenhydramine hydrochloride


General Information