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Pioglitazone
Pioglitazone - 51079-515-20 - (pioglitazone)
Drug Information of Pioglitazone
| Product NDC: | 51079-515 |
| Proprietary Name: | Pioglitazone |
| Non Proprietary Name: | pioglitazone |
| Active Ingredient(s): | 45 mg/1 & nbsp; pioglitazone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pioglitazone
| Product NDC: | 51079-515 |
| Labeler Name: | Mylan Institutional Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076801 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120907 |
Package Information of Pioglitazone
| Package NDC: | 51079-515-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-515-20) > 1 TABLET in 1 BLISTER PACK (51079-515-01) |
NDC Information of Pioglitazone
| NDC Code | 51079-515-20 |
| Proprietary Name | Pioglitazone |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-515-20) > 1 TABLET in 1 BLISTER PACK (51079-515-01) |
| Product NDC | 51079-515 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | pioglitazone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120907 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional Inc. |
| Substance Name | PIOGLITAZONE HYDROCHLORIDE |
| Strength Number | 45 |
| Strength Unit | mg/1 |
| Pharmaceutical 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] |
