Package 68001-361-03

Brand: montelukast

Generic: montelukast
NDC Package

Package Facts

Identity

Package NDC 68001-361-03
Digits Only 6800136103
Product NDC 68001-361
Description

500 TABLET in 1 BOTTLE (68001-361-03)

Marketing

Marketing Status
Marketed Since 2018-06-29
Brand montelukast
Generic montelukast
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d9dbbe03-bcc4-1af7-e053-2a95a90a8053", "openfda": {"upc": ["0368001361040", "0368001361033", "0368001361057"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["4c411d3e-47b6-481b-b846-419ed4cbb947"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (68001-361-03)", "package_ndc": "68001-361-03", "marketing_start_date": "20180629"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68001-361-04)", "package_ndc": "68001-361-04", "marketing_start_date": "20180629"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68001-361-05)", "package_ndc": "68001-361-05", "marketing_start_date": "20180629"}], "brand_name": "Montelukast", "product_id": "68001-361_d9dbbe03-bcc4-1af7-e053-2a95a90a8053", "dosage_form": "TABLET", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "68001-361", "generic_name": "Montelukast", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA203366", "marketing_category": "ANDA", "marketing_start_date": "20180629", "listing_expiration_date": "20261231"}