NDC Code |
51991-710-90 |
Proprietary Name |
pioglitazone hydrochloride |
Package Description |
90 TABLET in 1 BOTTLE (51991-710-90) |
Product NDC |
51991-710 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
pioglitazone hydrochloride |
Dosage Form Name |
TABLET |
Route Name |
ORAL |
Start Marketing Date |
20130213 |
Marketing Category Name |
ANDA |
Labeler Name |
Breckenridge Pharmaceutical, Inc. |
Substance Name |
PIOGLITAZONE HYDROCHLORIDE |
Strength Number |
45 |
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] |