| NDC Code | 0093-0154-05 |
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| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0093-0154-05) |
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| Product NDC | 0093-0154 |
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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 | 19990907 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075149 |
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| Manufacturer | Teva Pharmaceuticals USA Inc |
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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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