"70934-619-30" National Drug Code (NDC)

NDC Code	70934-619-30
Package Description	30 TABLET in 1 BOTTLE, PLASTIC (70934-619-30)
Product NDC	70934-619
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20200730
Marketing Category Name	ANDA
Application Number	ANDA077210
Manufacturer	Denton Pharma, Inc. dba Northwind Pharmaceuticals
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]