| NDC Code | 0378-0357-05 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0378-0357-05) |
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| Product NDC | 0378-0357 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pentoxifylline |
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| Non-Proprietary Name | Pentoxifylline |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 19970708 |
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| End Marketing Date | 20190531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074425 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | PENTOXIFYLLINE |
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| Strength | 400 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE] |
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