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Meclizine Hydrochloride - 42291-608-10 - (Meclizine)

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Drug Information of Meclizine Hydrochloride

Product NDC: 42291-608
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: 42291-608
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201451
Marketing Category: ANDA
Start Marketing Date: 20120504

Package Information of Meclizine Hydrochloride

Package NDC: 42291-608-10
Package Description: 1000 TABLET in 1 BOTTLE (42291-608-10)

NDC Information of Meclizine Hydrochloride

NDC Code 42291-608-10
Proprietary Name Meclizine Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (42291-608-10)
Product NDC 42291-608
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meclizine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120504
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
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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