"51991-891-33" National Drug Code (NDC)

NDC Code	51991-891-33
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (51991-891-33)
Product NDC	51991-891
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Erlotinib
Non-Proprietary Name	Erlotinib Hydrochloride
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20191105
End Marketing Date	20250731
Marketing Category Name	ANDA
Application Number	ANDA208488
Manufacturer	Breckenridge Pharmaceutical, Inc.
Substance Name	ERLOTINIB HYDROCHLORIDE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]