| NDC Code | 0378-1550-10 |
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| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1550-10) |
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| Product NDC | 0378-1550 |
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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 | 20120817 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090406 |
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| Manufacturer | Mylan Pharmaceuticals 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 | Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC],Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [Chemical/Ingredient],PPAR gamma [Chemical/Ingredient],Thiazolidinedione [EPC],Thiazolidinediones [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
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