"72606-572-01" National Drug Code (NDC)

NDC Code	72606-572-01
Package Description	30 TABLET in 1 BOTTLE (72606-572-01)
Product NDC	72606-572
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone Hydrochloride
Non-Proprietary Name	Pioglitazone Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20201028
Marketing Category Name	ANDA
Application Number	ANDA076798
Manufacturer	CELLTRION USA, INC.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	45
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]