"68788-7989-3" National Drug Code (NDC)

NDC Code	68788-7989-3
Package Description	30 TABLET in 1 BOTTLE (68788-7989-3)
Product NDC	68788-7989
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20210827
Marketing Category Name	ANDA
Application Number	ANDA077210
Manufacturer	Preferred Pharmaceuticals, Inc.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	15
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]