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Motion Sickness - 59779-198-07 - (Dimenhydrinate)

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Drug Information of Motion Sickness

Product NDC: 59779-198
Proprietary Name: Motion Sickness
Non Proprietary Name: Dimenhydrinate
Active Ingredient(s): 50    mg/1 & nbsp;   Dimenhydrinate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Motion Sickness

Product NDC: 59779-198
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19921201

Package Information of Motion Sickness

Package NDC: 59779-198-07
Package Description: 1 BLISTER PACK in 1 CARTON (59779-198-07) > 36 TABLET in 1 BLISTER PACK

NDC Information of Motion Sickness

NDC Code 59779-198-07
Proprietary Name Motion Sickness
Package Description 1 BLISTER PACK in 1 CARTON (59779-198-07) > 36 TABLET in 1 BLISTER PACK
Product NDC 59779-198
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dimenhydrinate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19921201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name DIMENHYDRINATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Motion Sickness


General Information