Package 72205-080-30

Brand: erlotinib hydrochloride

Generic: erlotinib hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72205-080-30
Digits Only 7220508030
Product NDC 72205-080
Product ID 72205-080_4cff04f5-3693-4d87-a9f8-a2b195e3d26e
Description

1 BOTTLE in 1 CARTON (72205-080-30) / 30 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2021-05-11
Brand erlotinib hydrochloride
Generic erlotinib hydrochloride
Sample Package No

Linked Drug Pages (1)

Erlotinib Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4cff04f5-3693-4d87-a9f8-a2b195e3d26e", "openfda": {"upc": ["0372205081307", "0372205082304", "0372205080300"], "unii": ["DA87705X9K"], "rxcui": ["603203", "603206", "603208"], "spl_set_id": ["4cff04f5-3693-4d87-a9f8-a2b195e3d26e"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72205-080-30)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "72205-080-30", "marketing_start_date": "20210511"}], "brand_name": "Erlotinib Hydrochloride", "product_id": "72205-080_4cff04f5-3693-4d87-a9f8-a2b195e3d26e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "72205-080", "generic_name": "Erlotinib Hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Erlotinib Hydrochloride", "active_ingredients": [{"name": "ERLOTINIB HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA214366", "marketing_category": "ANDA", "marketing_start_date": "20210511", "listing_expiration_date": "20261231"}