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Dramamine
Dramamine - 50580-313-36 - (Dimenhydrinate)
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: | 50580-313-36 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (50580-313-36) > 12 TABLET in 1 BLISTER PACK |
NDC Information of Dramamine
| NDC Code | 50580-313-36 |
| Proprietary Name | Dramamine |
| Package Description | 3 BLISTER PACK in 1 CARTON (50580-313-36) > 12 TABLET in 1 BLISTER PACK |
| 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 |
