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Meclizine Hydrochloride - 21695-237-90 - (Meclizine Hydrochloride)

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Drug Information of Meclizine Hydrochloride

Product NDC: 21695-237
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: 21695-237
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087128
Marketing Category: ANDA
Start Marketing Date: 19810603

Package Information of Meclizine Hydrochloride

Package NDC: 21695-237-90
Package Description: 90 TABLET in 1 BOTTLE (21695-237-90)

NDC Information of Meclizine Hydrochloride

NDC Code 21695-237-90
Proprietary Name Meclizine Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (21695-237-90)
Product NDC 21695-237
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 Rebel Distributors Corp.
Substance Name MECLIZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Antiemetic [EPC],Emesis Suppression [PE]

Complete Information of Meclizine Hydrochloride


General Information