| NDC Code | 70518-1882-0 |
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| Package Description | 30 POUCH in 1 BOX, UNIT-DOSE (70518-1882-0) > 1 TABLET in 1 POUCH (70518-1882-1) |
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| Product NDC | 70518-1882 |
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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 | 20190219 |
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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 | 45 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [CS],PPAR gamma [CS],Thiazolidinedione [EPC],Thiazolidinediones [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC] |
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