| Product NDC: | 54868-5913 |
| Proprietary Name: | Clemastine Fumarate |
| Non Proprietary Name: | Clemastine Fumarate |
| Active Ingredient(s): | 1.34 mg/1 & nbsp; Clemastine Fumarate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54868-5913 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA073458 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080627 |
| Package NDC: | 54868-5913-0 |
| Package Description: | 100 TABLET in 1 BOTTLE (54868-5913-0) |
| NDC Code | 54868-5913-0 |
| Proprietary Name | Clemastine Fumarate |
| Package Description | 100 TABLET in 1 BOTTLE (54868-5913-0) |
| Product NDC | 54868-5913 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Clemastine Fumarate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080627 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | CLEMASTINE FUMARATE |
| Strength Number | 1.34 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |