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MECLIZINE HYDROCHLORIDE - 52959-033-10 - (Meclizine Hydrocloride)

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Drug Information of MECLIZINE HYDROCHLORIDE

Product NDC: 52959-033
Proprietary Name: MECLIZINE HYDROCHLORIDE
Non Proprietary Name: Meclizine Hydrocloride
Active Ingredient(s): 25    mg/1 & nbsp;   Meclizine Hydrocloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of MECLIZINE HYDROCHLORIDE

Product NDC: 52959-033
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040659
Marketing Category: ANDA
Start Marketing Date: 20100604

Package Information of MECLIZINE HYDROCHLORIDE

Package NDC: 52959-033-10
Package Description: 10 TABLET in 1 BOTTLE (52959-033-10)

NDC Information of MECLIZINE HYDROCHLORIDE

NDC Code 52959-033-10
Proprietary Name MECLIZINE HYDROCHLORIDE
Package Description 10 TABLET in 1 BOTTLE (52959-033-10)
Product NDC 52959-033
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meclizine Hydrocloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100604
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
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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