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Meclizine Hydrochloride - 0781-1375-01 - (Meclizine Hydrochloride)

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Drug Information of Meclizine Hydrochloride

Product NDC: 0781-1375
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: 0781-1375
Labeler Name: Sandoz Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19890522

Package Information of Meclizine Hydrochloride

Package NDC: 0781-1375-01
Package Description: 100 TABLET in 1 BOTTLE (0781-1375-01)

NDC Information of Meclizine Hydrochloride

NDC Code 0781-1375-01
Proprietary Name Meclizine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (0781-1375-01)
Product NDC 0781-1375
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Meclizine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19890522
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Sandoz Inc
Substance Name MECLIZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Meclizine Hydrochloride


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