"70771-1022-5" National Drug Code (NDC)

NDC Code	70771-1022-5
Package Description	500 TABLET in 1 BOTTLE (70771-1022-5)
Product NDC	70771-1022
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20161116
Marketing Category Name	ANDA
Application Number	ANDA202456
Manufacturer	Zydus Lifesciences Limited
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	30
Strength Unit	mg/1
Pharmacy Classes	Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]