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Motion Sickness Relief - 59779-404-21 - (Meclizine HCl)

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Drug Information of Motion Sickness Relief

Product NDC: 59779-404
Proprietary Name: Motion Sickness Relief
Non Proprietary Name: Meclizine HCl
Active Ingredient(s): 25    mg/1 & nbsp;   Meclizine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Motion Sickness Relief

Product NDC: 59779-404
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20020529

Package Information of Motion Sickness Relief

Package NDC: 59779-404-21
Package Description: 1 BLISTER PACK in 1 CARTON (59779-404-21) > 16 TABLET, CHEWABLE in 1 BLISTER PACK

NDC Information of Motion Sickness Relief

NDC Code 59779-404-21
Proprietary Name Motion Sickness Relief
Package Description 1 BLISTER PACK in 1 CARTON (59779-404-21) > 16 TABLET, CHEWABLE in 1 BLISTER PACK
Product NDC 59779-404
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Meclizine HCl
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20020529
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name MECLIZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Motion Sickness Relief


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