Antivert - 0049-2140-66 - (meclizine hydrochloride)

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Drug Information of Antivert

Product NDC: 0049-2140
Proprietary Name: Antivert
Non Proprietary Name: meclizine hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   meclizine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Antivert

Product NDC: 0049-2140
Labeler Name: Roerig
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA010721
Marketing Category: NDA
Start Marketing Date: 19970411

Package Information of Antivert

Package NDC: 0049-2140-66
Package Description: 100 TABLET in 1 BOTTLE (0049-2140-66)

NDC Information of Antivert

NDC Code 0049-2140-66
Proprietary Name Antivert
Package Description 100 TABLET in 1 BOTTLE (0049-2140-66)
Product NDC 0049-2140
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name meclizine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970411
Marketing Category Name NDA
Labeler Name Roerig
Substance Name MECLIZINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Antiemetic [EPC],Emesis Suppression [PE]

Complete Information of Antivert


General Information