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GEMFIBROZIL
GEMFIBROZIL - 0115-9911-02 - (GEMFIBROZIL)
Drug Information of GEMFIBROZIL
| Product NDC: | 0115-9911 |
| Proprietary Name: | GEMFIBROZIL |
| Non Proprietary Name: | GEMFIBROZIL |
| Active Ingredient(s): | 600 mg/1 & nbsp; GEMFIBROZIL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GEMFIBROZIL
| Product NDC: | 0115-9911 |
| Labeler Name: | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078207 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091001 |
Package Information of GEMFIBROZIL
| Package NDC: | 0115-9911-02 |
| Package Description: | 500 TABLET, COATED in 1 BOTTLE (0115-9911-02) |
NDC Information of GEMFIBROZIL
| NDC Code | 0115-9911-02 |
| Proprietary Name | GEMFIBROZIL |
| Package Description | 500 TABLET, COATED in 1 BOTTLE (0115-9911-02) |
| Product NDC | 0115-9911 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GEMFIBROZIL |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | ANDA |
| Labeler Name | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Substance Name | GEMFIBROZIL |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient] |
