| NDC Code | 70518-1638-0 |
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| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1638-0) |
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| Product NDC | 70518-1638 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pioglitazone Hydrochloride |
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| Non-Proprietary Name | Pioglitazone Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20181106 |
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| End Marketing Date | 20251031 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200044 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | PIOGLITAZONE HYDROCHLORIDE |
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| Strength | 30 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS] |
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