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Meclizine HCl - 68788-0118-3 - (Meclizine HCl)

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Drug Information of Meclizine HCl

Product NDC: 68788-0118
Proprietary Name: Meclizine HCl
Non Proprietary Name: Meclizine HCl
Active Ingredient(s): 25    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: 68788-0118
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121213

Package Information of Meclizine HCl

Package NDC: 68788-0118-3
Package Description: 30 TABLET in 1 BOTTLE (68788-0118-3)

NDC Information of Meclizine HCl

NDC Code 68788-0118-3
Proprietary Name Meclizine HCl
Package Description 30 TABLET in 1 BOTTLE (68788-0118-3)
Product NDC 68788-0118
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Meclizine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121213
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name MECLIZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Meclizine HCl


General Information