| NDC Code | 68788-6846-9 |
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| Package Description | 90 TABLET in 1 BOTTLE (68788-6846-9) |
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| Product NDC | 68788-6846 |
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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 | 20161207 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200044 |
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| Manufacturer | Preferred Pharmaceuticals 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-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] |
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