Package 68071-4047-3

Brand: montelukast sodium

Generic: montelukast sodium
NDC Package

Package Facts

Identity

Package NDC 68071-4047-3
Digits Only 6807140473
Product NDC 68071-4047
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-4047-3)

Marketing

Marketing Status
Marketed Since 2017-08-10
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": "1d7a4391-15ea-178a-e063-6294a90a80c1", "openfda": {"upc": ["0368071404739"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["566a8fd7-fc00-2297-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4047-3)", "package_ndc": "68071-4047-3", "marketing_start_date": "20170810"}], "brand_name": "Montelukast Sodium", "product_id": "68071-4047_1d7a4391-15ea-178a-e063-6294a90a80c1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "68071-4047", "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": "ANDA202717", "marketing_category": "ANDA", "marketing_start_date": "20130411", "listing_expiration_date": "20261231"}