Package 72485-219-30

Brand: erlotinib

Generic: erlotinib hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72485-219-30
Digits Only 7248521930
Product NDC 72485-219
Product ID 72485-219_e7a350dc-b9b0-4650-9cb6-2948162a8e04
Description

1 BOTTLE in 1 BOX (72485-219-30) / 30 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-11-06
Brand erlotinib
Generic erlotinib hydrochloride
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": "e7a350dc-b9b0-4650-9cb6-2948162a8e04", "openfda": {"upc": ["0372485219308"], "unii": ["DA87705X9K"], "rxcui": ["603206"], "spl_set_id": ["766baa46-1916-44e8-b599-33017a4194f1"], "manufacturer_name": ["Armas Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (72485-219-30)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "72485-219-30", "marketing_start_date": "20191106"}], "brand_name": "Erlotinib", "product_id": "72485-219_e7a350dc-b9b0-4650-9cb6-2948162a8e04", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "72485-219", "generic_name": "Erlotinib hydrochloride", "labeler_name": "Armas Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Erlotinib", "active_ingredients": [{"name": "ERLOTINIB HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA211960", "marketing_category": "ANDA", "marketing_start_date": "20191106", "listing_expiration_date": "20261231"}