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Meclizine Hydrochloride - 68084-491-01 - (meclizine hydrochloride)

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Drug Information of Meclizine Hydrochloride

Product NDC: 68084-491
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: 68084-491
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201451
Marketing Category: ANDA
Start Marketing Date: 20110701

Package Information of Meclizine Hydrochloride

Package NDC: 68084-491-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-491-01) > 10 TABLET in 1 BLISTER PACK (68084-491-11)

NDC Information of Meclizine Hydrochloride

NDC Code 68084-491-01
Proprietary Name Meclizine Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-491-01) > 10 TABLET in 1 BLISTER PACK (68084-491-11)
Product NDC 68084-491
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name meclizine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110701
Marketing Category Name ANDA
Labeler Name American Health Packaging
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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