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Motion Sickness - 24385-004-12 - (Dimenhydrinate)

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Drug Information of Motion Sickness

Product NDC: 24385-004
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: 24385-004
Labeler Name: Amerisourcebergen Drug Corporation (Good Neighbour Pharmacy)
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100709

Package Information of Motion Sickness

Package NDC: 24385-004-12
Package Description: 12 BLISTER PACK in 1 CARTON (24385-004-12) > 12 TABLET in 1 BLISTER PACK

NDC Information of Motion Sickness

NDC Code 24385-004-12
Proprietary Name Motion Sickness
Package Description 12 BLISTER PACK in 1 CARTON (24385-004-12) > 12 TABLET in 1 BLISTER PACK
Product NDC 24385-004
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dimenhydrinate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100709
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Amerisourcebergen Drug Corporation (Good Neighbour Pharmacy)
Substance Name DIMENHYDRINATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Motion Sickness


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