NDC Code |
67046-231-30 |
Proprietary Name |
Gemfibrozil |
Package Description |
30 TABLET, FILM COATED in 1 BLISTER PACK (67046-231-30) |
Product NDC |
67046-231 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Gemfibrozil |
Dosage Form Name |
TABLET, FILM COATED |
Route Name |
ORAL |
Start Marketing Date |
20101109 |
Marketing Category Name |
ANDA |
Labeler Name |
Contract Pharmacy Services-PA |
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] |