NDC Code |
0615-3559-39 |
Proprietary Name |
Gemfibrozil |
Package Description |
30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3559-39) |
Product NDC |
0615-3559 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Gemfibrozil |
Dosage Form Name |
TABLET, FILM COATED |
Route Name |
ORAL |
Start Marketing Date |
19931124 |
Marketing Category Name |
ANDA |
Labeler Name |
NCS HealthCare of KY, Inc dba Vangard Labs |
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] |