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Meclizine Hydrochloride - 51079-090-20 - (meclizine hydrochloride)

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Drug Information of Meclizine Hydrochloride

Product NDC: 51079-090
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: 51079-090
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087128
Marketing Category: ANDA
Start Marketing Date: 20110513

Package Information of Meclizine Hydrochloride

Package NDC: 51079-090-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-090-20) > 1 TABLET in 1 BLISTER PACK (51079-090-01)

NDC Information of Meclizine Hydrochloride

NDC Code 51079-090-20
Proprietary Name Meclizine Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-090-20) > 1 TABLET in 1 BLISTER PACK (51079-090-01)
Product NDC 51079-090
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name meclizine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110513
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
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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