Package 68645-560-54

Brand: montelukast

Generic: montelukast
NDC Package

Package Facts

Identity

Package NDC 68645-560-54
Digits Only 6864556054
Product NDC 68645-560
Product ID 68645-560_474399e6-7a3d-2d8a-e063-6294a90a7692
Description

30 TABLET, FILM COATED in 1 BOTTLE (68645-560-54)

Marketing

Marketing Status
Marketed Since 2014-09-10
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": "474399e6-7a3d-2d8a-e063-6294a90a7692", "openfda": {"upc": ["0368645560540"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["b7182fd7-c018-401d-ad24-c0a2cc8d1c58"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68645-560-54)", "package_ndc": "68645-560-54", "marketing_start_date": "20140910"}], "brand_name": "Montelukast", "product_id": "68645-560_474399e6-7a3d-2d8a-e063-6294a90a7692", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "68645-560", "generic_name": "Montelukast", "labeler_name": "Legacy Pharmaceutical Packaging, 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": "20140910", "listing_expiration_date": "20261231"}