Dramamine - 50580-313-12 - (Dimenhydrinate)

Alphabetical Index


Drug Information of Dramamine

Product NDC: 50580-313
Proprietary Name: Dramamine
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 Dramamine

Product NDC: 50580-313
Labeler Name: McNeil Consumer Healthcare Div McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20081001

Package Information of Dramamine

Package NDC: 50580-313-12
Package Description: 1 VIAL, PLASTIC in 1 BLISTER PACK (50580-313-12) > 12 TABLET in 1 VIAL, PLASTIC

NDC Information of Dramamine

NDC Code 50580-313-12
Proprietary Name Dramamine
Package Description 1 VIAL, PLASTIC in 1 BLISTER PACK (50580-313-12) > 12 TABLET in 1 VIAL, PLASTIC
Product NDC 50580-313
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dimenhydrinate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081001
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance Name DIMENHYDRINATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Dramamine


General Information