Package 68071-5278-3

Brand: montelukast sodium

Generic: montelukast sodium
NDC Package

Package Facts

Identity

Package NDC 68071-5278-3
Digits Only 6807152783
Product NDC 68071-5278
Product ID 68071-5278_2a80536c-27fd-0142-e063-6294a90a458f
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-5278-3)

Marketing

Marketing Status
Marketed Since 2020-06-10
Brand montelukast sodium
Generic montelukast sodium
Sample Package No

Linked Drug Pages (1)

montelukast sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a80536c-27fd-0142-e063-6294a90a458f", "openfda": {"upc": ["0368071527834"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["a7c11cbe-0834-27a5-e053-2995a90ac43f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-5278-3)", "package_ndc": "68071-5278-3", "marketing_start_date": "20200610"}], "brand_name": "montelukast sodium", "product_id": "68071-5278_2a80536c-27fd-0142-e063-6294a90a458f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "68071-5278", "generic_name": "montelukast sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "montelukast sodium", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA204290", "marketing_category": "ANDA", "marketing_start_date": "20160101", "listing_expiration_date": "20261231"}