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MECLIZINE HYDROCHLORIDE - 52125-578-20 - (Meclizine Hydrocloride)

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Drug Information of MECLIZINE HYDROCHLORIDE

Product NDC: 52125-578
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: 52125-578
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040659
Marketing Category: ANDA
Start Marketing Date: 20130524

Package Information of MECLIZINE HYDROCHLORIDE

Package NDC: 52125-578-20
Package Description: 100 TABLET in 1 VIAL (52125-578-20)

NDC Information of MECLIZINE HYDROCHLORIDE

NDC Code 52125-578-20
Proprietary Name MECLIZINE HYDROCHLORIDE
Package Description 100 TABLET in 1 VIAL (52125-578-20)
Product NDC 52125-578
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meclizine Hydrocloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130524
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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