| NDC Code | 68084-878-01 |
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| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-878-01) > 1 TABLET in 1 BLISTER PACK (68084-878-11) |
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| Product NDC | 68084-878 |
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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 | 20150730 |
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| End Marketing Date | 20181130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076798 |
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| Manufacturer | American Health Packaging |
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| Substance Name | PIOGLITAZONE HYDROCHLORIDE |
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| Strength | 15 |
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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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