| NDC Code | 51991-709-33 |
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| Package Description | 30 TABLET in 1 BOTTLE (51991-709-33) |
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| Product NDC | 51991-709 |
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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 | 20130213 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078472 |
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| Manufacturer | Breckenridge Pharmaceutical, 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 | 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] |
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