Package 69339-168-03

Brand: gefitinib

Generic: gefitinib
NDC Package

Package Facts

Identity

Package NDC 69339-168-03
Digits Only 6933916803
Product NDC 69339-168
Description

30 TABLET, FILM COATED in 1 BOTTLE (69339-168-03)

Marketing

Marketing Status
Marketed Since 2023-06-05
Brand gefitinib
Generic gefitinib
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "210d9dcf-53f2-4dba-9d4e-6a072a153777", "openfda": {"nui": ["N0000175605", "N0000175076"], "upc": ["0369339168035"], "unii": ["S65743JHBS"], "rxcui": ["349472"], "spl_set_id": ["1a3c0ce7-06a1-4e04-9106-14ddb2a866a5"], "pharm_class_epc": ["Kinase Inhibitor [EPC]"], "pharm_class_moa": ["Protein Kinase Inhibitors [MoA]"], "manufacturer_name": ["Natco Pharma USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69339-168-03)", "package_ndc": "69339-168-03", "marketing_start_date": "20230605"}], "brand_name": "Gefitinib", "product_id": "69339-168_210d9dcf-53f2-4dba-9d4e-6a072a153777", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "69339-168", "generic_name": "Gefitinib", "labeler_name": "Natco Pharma USA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gefitinib", "active_ingredients": [{"name": "GEFITINIB", "strength": "250 mg/1"}], "application_number": "ANDA212827", "marketing_category": "ANDA", "marketing_start_date": "20230605", "listing_expiration_date": "20271231"}