Package 67296-1926-3

Brand: montelukast sodium

Generic: montelukast sodium
NDC Package

Package Facts

Identity

Package NDC 67296-1926-3
Digits Only 6729619263
Product NDC 67296-1926
Product ID 67296-1926_4727cc05-2fd8-7524-e063-6394a90a398f
Description

30 TABLET, FILM COATED in 1 BOTTLE (67296-1926-3)

Marketing

Marketing Status
Marketed Since 2013-06-11
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": "4727cc05-2fd8-7524-e063-6394a90a398f", "openfda": {"upc": ["0316729119108"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["2fbdf1be-a37f-879b-e063-6394a90aa20d"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67296-1926-3)", "package_ndc": "67296-1926-3", "marketing_start_date": "20130611"}], "brand_name": "Montelukast Sodium", "product_id": "67296-1926_4727cc05-2fd8-7524-e063-6394a90a398f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "67296-1926", "generic_name": "Montelukast Sodium", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast Sodium", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA202717", "marketing_category": "ANDA", "marketing_start_date": "20130411", "listing_expiration_date": "20261231"}