Package 68071-3355-9

Brand: montelukast sodium

Generic: montelukast sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3355-9
Digits Only 6807133559
Product NDC 68071-3355
Product ID 68071-3355_1ce908ef-4d89-b74f-e063-6394a90a80f0
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-3355-9)

Marketing

Marketing Status
Marketed Since 2017-07-18
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": "1ce908ef-4d89-b74f-e063-6394a90a80f0", "openfda": {"upc": ["0368071335590"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["549f1d1a-81f5-29f5-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3355-9)", "package_ndc": "68071-3355-9", "marketing_start_date": "20170718"}], "brand_name": "Montelukast Sodium", "product_id": "68071-3355_1ce908ef-4d89-b74f-e063-6394a90a80f0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "68071-3355", "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"}