| NDC Code | 53002-1756-9 |
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| Package Description | 90 TABLET in 1 BOTTLE (53002-1756-9) |
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| Product NDC | 53002-1756 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pioglitazonehydrochloride |
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| Non-Proprietary Name | Pioglitazonehydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20130213 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091298 |
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| Manufacturer | RPK Pharmaceuticals, 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 | PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS] |
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