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Dimenhydrinate
Dimenhydrinate - 0603-3327-32 - (Dimenhydrinate)
Drug Information of Dimenhydrinate
| Product NDC: | 0603-3327 |
| Proprietary Name: | Dimenhydrinate |
| 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 Dimenhydrinate
| Product NDC: | 0603-3327 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040301 |
Package Information of Dimenhydrinate
| Package NDC: | 0603-3327-32 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-3327-32) |
NDC Information of Dimenhydrinate
| NDC Code | 0603-3327-32 |
| Proprietary Name | Dimenhydrinate |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-3327-32) |
| Product NDC | 0603-3327 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dimenhydrinate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | DIMENHYDRINATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
