"82968-002-01" National Drug Code (NDC)

NDC Code	82968-002-01
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (82968-002-01)
Product NDC	82968-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Tadalafil
Non-Proprietary Name	Tadalafil
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20240821
Marketing Category Name	ANDA
Application Number	ANDA217606
Manufacturer	FOURRTS (INDIA) LABORATORIES PRIVATE LIMITED
Substance Name	TADALAFIL
Strength	5
Strength Unit	mg/1
Pharmacy Classes	Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]