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Pioglitazone and metformin
Pioglitazone and metformin - 0781-5627-06 - (Pioglitazone and metformin)
Drug Information of Pioglitazone and metformin
| Product NDC: | 0781-5627 |
| Proprietary Name: | Pioglitazone and metformin |
| Non Proprietary Name: | Pioglitazone and metformin |
| Active Ingredient(s): | 850; 15 mg/1; mg/1 & nbsp; Pioglitazone and metformin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pioglitazone and metformin
| Product NDC: | 0781-5627 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091273 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130502 |
Package Information of Pioglitazone and metformin
| Package NDC: | 0781-5627-06 |
| Package Description: | 5 TABLET, FILM COATED in 1 BLISTER PACK (0781-5627-06) |
NDC Information of Pioglitazone and metformin
| NDC Code | 0781-5627-06 |
| Proprietary Name | Pioglitazone and metformin |
| Package Description | 5 TABLET, FILM COATED in 1 BLISTER PACK (0781-5627-06) |
| Product NDC | 0781-5627 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pioglitazone and metformin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130502 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE |
| Strength Number | 850; 15 |
| Strength Unit | mg/1; 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],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
