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Meclizine Hydrochloride - 55154-5864-9 - (meclizine hydrochloride)

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Drug Information of Meclizine Hydrochloride

Product NDC: 55154-5864
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: 55154-5864
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087128
Marketing Category: ANDA
Start Marketing Date: 19810603

Package Information of Meclizine Hydrochloride

Package NDC: 55154-5864-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-5864-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Meclizine Hydrochloride

NDC Code 55154-5864-9
Proprietary Name Meclizine Hydrochloride
Package Description 6 BLISTER PACK in 1 CARTON (55154-5864-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-5864
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name meclizine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19810603
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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