Package 63304-135-11

Brand: erlotinib

Generic: erlotinib
NDC Package

Package Facts

Identity

Package NDC 63304-135-11
Digits Only 6330413511
Product NDC 63304-135
Description

3 BLISTER PACK in 1 CARTON (63304-135-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-135-31)

Marketing

Marketing Status
Marketed Since 2019-11-05
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": "c160713b-c06f-49b4-80ea-fc1afb030b81", "openfda": {"nui": ["N0000175605", "N0000175076"], "upc": ["0363304095302"], "unii": ["J4T82NDH7E"], "rxcui": ["603203", "603206", "603208"], "spl_set_id": ["e36fa076-e23b-437f-bbd2-0433ce333175"], "pharm_class_epc": ["Kinase Inhibitor [EPC]"], "pharm_class_moa": ["Protein Kinase Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (63304-135-11)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-135-31)", "package_ndc": "63304-135-11", "marketing_start_date": "20191105"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63304-135-30)", "package_ndc": "63304-135-30", "marketing_start_date": "20191105"}], "brand_name": "Erlotinib", "product_id": "63304-135_c160713b-c06f-49b4-80ea-fc1afb030b81", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "63304-135", "generic_name": "Erlotinib", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Erlotinib", "active_ingredients": [{"name": "ERLOTINIB", "strength": "150 mg/1"}], "application_number": "ANDA210300", "marketing_category": "ANDA", "marketing_start_date": "20191105", "listing_expiration_date": "20261231"}