"50268-591-15" National Drug Code (NDC)

NDC Code	50268-591-15
Package Description	50 BLISTER PACK in 1 BOX (50268-591-15) > 1 CAPSULE in 1 BLISTER PACK (50268-591-11)
Product NDC	50268-591
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nifedipine
Non-Proprietary Name	Nifedipine
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20200914
End Marketing Date	20211130
Marketing Category Name	ANDA
Application Number	ANDA072781
Manufacturer	AvPAK
Substance Name	NIFEDIPINE
Strength	10
Strength Unit	mg/1
Pharmacy Classes	Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]