| NDC Code | 57664-327-88 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (57664-327-88) |
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| Product NDC | 57664-327 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ticlopidine Hydrochloride |
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| Non-Proprietary Name | Ticlopidine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20020926 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075526 |
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| Manufacturer | Caraco Pharmaceutical Laboratories, Ltd. |
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| Substance Name | TICLOPIDINE HYDROCHLORIDE |
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| Strength | 250 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC] |
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