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Meclizine HCl - 0536-3985-01 - (Meclizine HCl)

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Drug Information of Meclizine HCl

Product NDC: 0536-3985
Proprietary Name: Meclizine HCl
Non Proprietary Name: Meclizine HCl
Active Ingredient(s): 12.5    mg/1 & nbsp;   Meclizine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Meclizine HCl

Product NDC: 0536-3985
Labeler Name: Rugby Laboratories Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060714

Package Information of Meclizine HCl

Package NDC: 0536-3985-01
Package Description: 100 TABLET in 1 BOTTLE (0536-3985-01)

NDC Information of Meclizine HCl

NDC Code 0536-3985-01
Proprietary Name Meclizine HCl
Package Description 100 TABLET in 1 BOTTLE (0536-3985-01)
Product NDC 0536-3985
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Meclizine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060714
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rugby Laboratories Inc.
Substance Name MECLIZINE HYDROCHLORIDE
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Meclizine HCl


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