| NDC Code | 57664-327-13 |
|---|
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (57664-327-13) |
|---|
| Product NDC | 57664-327 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ticlopidine Hydrochloride |
|---|
| Non-Proprietary Name | Ticlopidine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20020926 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA075526 |
|---|
| Manufacturer | Caraco Pharmaceutical Laboratories, Ltd. |
|---|
| Substance Name | TICLOPIDINE HYDROCHLORIDE |
|---|
| Strength | 250 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC] |
|---|