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Clemastine Fumarate
Clemastine Fumarate - 0781-1359-01 - (Clemastine Fumarate)
Drug Information of Clemastine Fumarate
| Product NDC: | 0781-1359 |
| Proprietary Name: | Clemastine Fumarate |
| Non Proprietary Name: | Clemastine Fumarate |
| Active Ingredient(s): | 2.68 mg/1 & nbsp; Clemastine Fumarate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clemastine Fumarate
| Product NDC: | 0781-1359 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073459 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19931031 |
Package Information of Clemastine Fumarate
| Package NDC: | 0781-1359-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0781-1359-01) |
NDC Information of Clemastine Fumarate
| NDC Code | 0781-1359-01 |
| Proprietary Name | Clemastine Fumarate |
| Package Description | 100 TABLET in 1 BOTTLE (0781-1359-01) |
| Product NDC | 0781-1359 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clemastine Fumarate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19931031 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | CLEMASTINE FUMARATE |
| Strength Number | 2.68 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
