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Gemfibrozil
Gemfibrozil - 51079-787-19 - (Gemfibrozil)
Drug Information of Gemfibrozil
| Product NDC: | 51079-787 |
| Proprietary Name: | Gemfibrozil |
| Non Proprietary Name: | Gemfibrozil |
| Active Ingredient(s): | 600 mg/1 & nbsp; Gemfibrozil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gemfibrozil
| Product NDC: | 51079-787 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074256 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110823 |
Package Information of Gemfibrozil
| Package NDC: | 51079-787-19 |
| Package Description: | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-787-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-787-17) |
NDC Information of Gemfibrozil
| NDC Code | 51079-787-19 |
| Proprietary Name | Gemfibrozil |
| Package Description | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-787-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-787-17) |
| Product NDC | 51079-787 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Gemfibrozil |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110823 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL 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] |
