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Meclizine Hydrochloride - 65162-441-10 - (Meclizine)

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Drug Information of Meclizine Hydrochloride

Product NDC: 65162-441
Proprietary Name: Meclizine Hydrochloride
Non Proprietary Name: Meclizine
Active Ingredient(s): 12.5    mg/1 & nbsp;   Meclizine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Meclizine Hydrochloride

Product NDC: 65162-441
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201451
Marketing Category: ANDA
Start Marketing Date: 20100212

Package Information of Meclizine Hydrochloride

Package NDC: 65162-441-10
Package Description: 100 TABLET in 1 BOTTLE (65162-441-10)

NDC Information of Meclizine Hydrochloride

NDC Code 65162-441-10
Proprietary Name Meclizine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (65162-441-10)
Product NDC 65162-441
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meclizine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100212
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
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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