NDC Code |
13668-119-52 |
Proprietary Name |
PIOGLITAZONEHYDROCHLORIDE |
Package Description |
7000 TABLET in 1 BOTTLE (13668-119-52) |
Product NDC |
13668-119 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
PIOGLITAZONEHYDROCHLORIDE |
Dosage Form Name |
TABLET |
Route Name |
ORAL |
Start Marketing Date |
20130213 |
Marketing Category Name |
ANDA |
Labeler Name |
Torrent Pharmaceuticals Limited |
Substance Name |
PIOGLITAZONE HYDROCHLORIDE |
Strength Number |
30 |
Strength Unit |
mg/1 |
Pharmaceutical Classes |
Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC],Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [Chemical/Ingredient],PPAR gamma [Chemical/Ingredient],Thiazolidinedione [EPC],Thiazolidinediones [Chemical/Ingredient] |