Home
>
National Drug Code (NDC)
>
Gemfibrozil
Gemfibrozil - 16714-101-01 - (gemfibrozil)
Drug Information of Gemfibrozil
| Product NDC: | 16714-101 |
| Proprietary Name: | Gemfibrozil |
| Non Proprietary Name: | gemfibrozil |
| Active Ingredient(s): | 600 mg/1 & nbsp; gemfibrozil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gemfibrozil
| Product NDC: | 16714-101 |
| Labeler Name: | Northstar RxLLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079072 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101220 |
Package Information of Gemfibrozil
| Package NDC: | 16714-101-01 |
| Package Description: | 30 TABLET in 1 BOTTLE (16714-101-01) |
NDC Information of Gemfibrozil
| NDC Code | 16714-101-01 |
| Proprietary Name | Gemfibrozil |
| Package Description | 30 TABLET in 1 BOTTLE (16714-101-01) |
| Product NDC | 16714-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | gemfibrozil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101220 |
| Marketing Category Name | ANDA |
| Labeler Name | Northstar RxLLC |
| 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] |
