| NDC Code | 57237-217-81 |
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| Package Description | 180 TABLET, FILM COATED in 1 BOTTLE (57237-217-81) |
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| Product NDC | 57237-217 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pioglitazone Hydrochloride And Metformin Hydrochloride |
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| Non-Proprietary Name | Pioglitazone Hydrochloride And Metformin Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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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 | ANDA200823 |
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| Manufacturer | Rising Pharma Holdings, Inc. |
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| Substance Name | METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE |
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| Strength | 500; 15 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Biguanide [EPC], Biguanides [CS], 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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