Package 68071-4034-9

Brand: montelukast

Generic: montelukast
NDC Package

Package Facts

Identity

Package NDC 68071-4034-9
Digits Only 6807140349
Product NDC 68071-4034
Product ID 68071-4034_1d7a445a-3c64-0235-e063-6394a90add16
Description

90 TABLET in 1 BOTTLE (68071-4034-9)

Marketing

Marketing Status
Marketed Since 2017-08-08
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": "1d7a445a-3c64-0235-e063-6394a90add16", "openfda": {"upc": ["0368071403497"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["56429f04-97b6-06a9-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-4034-9)", "package_ndc": "68071-4034-9", "marketing_start_date": "20170808"}], "brand_name": "Montelukast", "product_id": "68071-4034_1d7a445a-3c64-0235-e063-6394a90add16", "dosage_form": "TABLET", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "68071-4034", "generic_name": "Montelukast", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA203366", "marketing_category": "ANDA", "marketing_start_date": "20120228", "listing_expiration_date": "20261231"}