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Meclizine Hydrochloride - 65162-442-11 - (Meclizine Hydrochloride)

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Drug Information of Meclizine Hydrochloride

Product NDC: 65162-442
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: 65162-442
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: 65162-442-11
Package Description: 1000 TABLET in 1 BOTTLE (65162-442-11)

NDC Information of Meclizine Hydrochloride

NDC Code 65162-442-11
Proprietary Name Meclizine Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (65162-442-11)
Product NDC 65162-442
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meclizine Hydrochloride
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 25
Strength Unit mg/1
Pharmaceutical Classes Antiemetic [EPC],Emesis Suppression [PE]

Complete Information of Meclizine Hydrochloride


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