NDC Active Ingredient Erlotinib Hydrochloride

NDC Proprietary Name Non-Proprietary Name Dosage Form Route Name Company Name Product Type
0093-7663Erlotinib ErlotinibTablet, Film CoatedOralTeva Pharmaceuticals Usa, Inc.Human Prescription Drug
0093-7664Erlotinib ErlotinibTablet, Film CoatedOralTeva Pharmaceuticals Usa, Inc.Human Prescription Drug
50242-062Tarceva Erlotinib HydrochlorideTabletOralGenentech, Inc.Human Prescription Drug
50242-063Tarceva Erlotinib HydrochlorideTabletOralGenentech, Inc.Human Prescription Drug
50242-064Tarceva Erlotinib HydrochlorideTabletOralGenentech, Inc.Human Prescription Drug
51991-890Erlotinib Erlotinib HydrochlorideTablet, Film CoatedOralBreckenridge Pharmaceutical, Inc.Human Prescription Drug
51991-891Erlotinib Erlotinib HydrochlorideTablet, Film CoatedOralBreckenridge Pharmaceutical, Inc.Human Prescription Drug
51991-892Erlotinib Erlotinib HydrochlorideTablet, Film CoatedOralBreckenridge Pharmaceutical, Inc.Human Prescription Drug
72485-217Erlotinib Erlotinib HydrochlorideTablet, Film CoatedOralArmas Pharmaceuticals Inc.Human Prescription Drug
72485-218Erlotinib Erlotinib HydrochlorideTablet, Film CoatedOralArmas Pharmaceuticals Inc.Human Prescription Drug
72485-219Erlotinib Erlotinib HydrochlorideTablet, Film CoatedOralArmas Pharmaceuticals Inc.Human Prescription Drug

There are 11 NDC products with the active ingredient ERLOTINIB HYDROCHLORIDE.