Package 0093-7663-56

Brand: erlotinib

Generic: erlotinib
NDC Package

Package Facts

Identity

Package NDC 0093-7663-56
Digits Only 0093766356
Product NDC 0093-7663
Product ID 0093-7663_4368f7b2-5bdb-4232-90b0-f6a769d71e9b
Description

30 TABLET, FILM COATED in 1 BOTTLE (0093-7663-56)

Marketing

Marketing Status
Marketed Since 2019-05-09
Brand erlotinib
Generic erlotinib
Sample Package No

Linked Drug Pages (1)

Erlotinib ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4368f7b2-5bdb-4232-90b0-f6a769d71e9b", "openfda": {"unii": ["DA87705X9K"], "rxcui": ["603203", "603206", "603208"], "spl_set_id": ["5d97f401-4853-4a9a-907d-21e8a4d16088"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-7663-56)", "package_ndc": "0093-7663-56", "marketing_start_date": "20190509"}], "brand_name": "Erlotinib", "product_id": "0093-7663_4368f7b2-5bdb-4232-90b0-f6a769d71e9b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "0093-7663", "generic_name": "Erlotinib", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Erlotinib", "active_ingredients": [{"name": "ERLOTINIB HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA091059", "marketing_category": "ANDA", "marketing_start_date": "20190509", "listing_expiration_date": "20261231"}