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Meclizine Hydrochloride - 52959-225-00 - (meclizine hydrochloride)

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Drug Information of Meclizine Hydrochloride

Product NDC: 52959-225
Proprietary Name: Meclizine Hydrochloride
Non Proprietary Name: meclizine hydrochloride
Active Ingredient(s): 12.5    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: 52959-225
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087127
Marketing Category: ANDA
Start Marketing Date: 19810603

Package Information of Meclizine Hydrochloride

Package NDC: 52959-225-00
Package Description: 100 TABLET in 1 BOTTLE (52959-225-00)

NDC Information of Meclizine Hydrochloride

NDC Code 52959-225-00
Proprietary Name Meclizine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (52959-225-00)
Product NDC 52959-225
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 H.J. Harkins Company, Inc.
Substance Name MECLIZINE HYDROCHLORIDE
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes Antiemetic [EPC],Emesis Suppression [PE]

Complete Information of Meclizine Hydrochloride


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