"0069-0231-01" National Drug Code (NDC)

NDC Code	0069-0231-01
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (0069-0231-01)
Product NDC	0069-0231
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lorbrena
Non-Proprietary Name	Lorlatinib
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20181119
Marketing Category Name	NDA
Application Number	NDA210868
Manufacturer	Pfizer Laboratories Div Pfizer Inc
Substance Name	LORLATINIB
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Breast Cancer Resistance Protein Inhibitors [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Kinase Inhibitor [EPC], Kinase Inhibitors [MoA], Multidrug and Toxin Extrusion Transporter 1 Inhibitors [MoA], Organic Anion Transporter 3 Inhibitors [MoA], Organic Cation Transporter 1 Inhibitors [MoA], P-Glycoprotein Inducers [MoA]