| NDC Code | 0093-7678-06 |
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| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (0093-7678-06) |
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| Product NDC | 0093-7678 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pioglitazone And Metformin Hydrochloride |
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| Non-Proprietary Name | Pioglitazone 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 | 20150204 |
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| End Marketing Date | 20190331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091155 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | PIOGLITAZONE HYDROCHLORIDE; METFORMIN HYDROCHLORIDE |
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| Strength | 15; 850 |
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| Strength Unit | mg/1; 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],Biguanide [EPC],Biguanides [CS] |
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