Package 31722-263-30

Brand: erlotinib

Generic: erlotinib
NDC Package

Package Facts

Identity

Package NDC 31722-263-30
Digits Only 3172226330
Product NDC 31722-263
Description

1 BOTTLE in 1 CARTON (31722-263-30) / 30 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-05-24
Brand erlotinib
Generic erlotinib
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1bca3db4-f885-5bed-e063-6294a90ae9fa", "openfda": {"upc": ["0331722264303", "0331722265300", "0331722263306"], "unii": ["DA87705X9K"], "rxcui": ["603203", "603206", "603208"], "spl_set_id": ["a3b2d622-b4d5-4819-862b-f8fd3adcec6f"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-263-30)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "31722-263-30", "marketing_start_date": "20240524"}], "brand_name": "ERLOTINIB", "product_id": "31722-263_1bca3db4-f885-5bed-e063-6294a90ae9fa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "31722-263", "generic_name": "ERLOTINIB", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ERLOTINIB", "active_ingredients": [{"name": "ERLOTINIB HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA209267", "marketing_category": "ANDA", "marketing_start_date": "20240524", "listing_expiration_date": "20261231"}