Package 82009-009-10

Brand: montelukast

Generic: montelukast
NDC Package

Package Facts

Identity

Package NDC 82009-009-10
Digits Only 8200900910
Product NDC 82009-009
Product ID 82009-009_2f3344ca-4170-1e1b-e063-6394a90a426b
Description

1000 TABLET, FILM COATED in 1 BOTTLE (82009-009-10)

Marketing

Marketing Status
Marketed Since 2022-06-07
Brand montelukast
Generic montelukast
Sample Package No

Linked Drug Pages (1)

Montelukast ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2f3344ca-4170-1e1b-e063-6394a90a426b", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["5d71088b-b0fa-4bf0-a6e7-6163bd9e0dd4"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (82009-009-10)", "package_ndc": "82009-009-10", "marketing_start_date": "20220607"}], "brand_name": "Montelukast", "product_id": "82009-009_2f3344ca-4170-1e1b-e063-6394a90a426b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "82009-009", "generic_name": "Montelukast", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA202843", "marketing_category": "ANDA", "marketing_start_date": "20220607", "listing_expiration_date": "20261231"}