NDC Code |
0115-9911-13 |
Proprietary Name |
GEMFIBROZIL |
Package Description |
60 TABLET, COATED in 1 BOTTLE (0115-9911-13) |
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] |