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Meclizine Hydrochloride - 50436-3988-1 - (meclizine hydrochloride)

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Drug Information of Meclizine Hydrochloride

Product NDC: 50436-3988
Proprietary Name: Meclizine Hydrochloride
Non Proprietary Name: meclizine hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   meclizine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Meclizine Hydrochloride

Product NDC: 50436-3988
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087128
Marketing Category: ANDA
Start Marketing Date: 19810603

Package Information of Meclizine Hydrochloride

Package NDC: 50436-3988-1
Package Description: 30 TABLET in 1 BOTTLE (50436-3988-1)

NDC Information of Meclizine Hydrochloride

NDC Code 50436-3988-1
Proprietary Name Meclizine Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (50436-3988-1)
Product NDC 50436-3988
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name meclizine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19810603
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name MECLIZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Antiemetic [EPC],Emesis Suppression [PE]

Complete Information of Meclizine Hydrochloride


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