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DIMENHYDRINATE
DIMENHYDRINATE - 49483-352-36 - (DIMENHYDRINATE)
Drug Information of DIMENHYDRINATE
| Product NDC: | 49483-352 |
| Proprietary Name: | DIMENHYDRINATE |
| Non Proprietary Name: | DIMENHYDRINATE |
| Active Ingredient(s): | 50 mg/1 & nbsp; DIMENHYDRINATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIMENHYDRINATE
| Product NDC: | 49483-352 |
| Labeler Name: | Time Cap Labs, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110128 |
Package Information of DIMENHYDRINATE
| Package NDC: | 49483-352-36 |
| Package Description: | 36 TABLET, FILM COATED in 1 BLISTER PACK (49483-352-36) |
NDC Information of DIMENHYDRINATE
| NDC Code | 49483-352-36 |
| Proprietary Name | DIMENHYDRINATE |
| Package Description | 36 TABLET, FILM COATED in 1 BLISTER PACK (49483-352-36) |
| Product NDC | 49483-352 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIMENHYDRINATE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110128 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Time Cap Labs, Inc |
| Substance Name | DIMENHYDRINATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
