Package 72189-418-90

Brand: montelukast sodium

Generic: montelukast sodium
NDC Package

Package Facts

Identity

Package NDC 72189-418-90
Digits Only 7218941890
Product NDC 72189-418
Description

90 TABLET, FILM COATED in 1 BOTTLE (72189-418-90)

Marketing

Marketing Status
Marketed Since 2023-02-02
Brand montelukast sodium
Generic montelukast sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4d0d3f-0096-e010-e063-6294a90a1ae9", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["f3bdf2a3-d661-5128-e053-2995a90a4661"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-418-30)", "package_ndc": "72189-418-30", "marketing_start_date": "20230202"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-418-90)", "package_ndc": "72189-418-90", "marketing_start_date": "20230202"}], "brand_name": "MONTELUKAST SODIUM", "product_id": "72189-418_2c4d0d3f-0096-e010-e063-6294a90a1ae9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "72189-418", "generic_name": "MONTELUKAST SODIUM", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MONTELUKAST SODIUM", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA202843", "marketing_category": "ANDA", "marketing_start_date": "20230202", "listing_expiration_date": "20261231"}