"68382-307-06" National Drug Code (NDC)

NDC Code	68382-307-06
Package Description	30 TABLET in 1 BOTTLE (68382-307-06)
Product NDC	68382-307
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 Pharmaceuticals USA Inc.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	30
Strength Unit	mg/1
Pharmacy Classes	PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]