Erlotinib
NDC 63304-135 · Sun Pharmaceutical Industries, Inc.
Generic nameErlotinib
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ERLOTINIB
Strength150 mg/1
Pharmacologic classKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]
Marketing categoryANDA
Packages
63304-135-11 — 3 BLISTER PACK in 1 CARTON (63304-135-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-135-31)
63304-135-30 — 30 TABLET, FILM COATED in 1 BOTTLE (63304-135-30)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.