Package 68071-3855-3

Brand: montelukast

Generic: montelukast
NDC Package

Package Facts

Identity

Package NDC 68071-3855-3
Digits Only 6807138553
Product NDC 68071-3855
Product ID 68071-3855_365e27d8-b610-c19e-e063-6394a90a3610
Description

30 TABLET in 1 BOTTLE (68071-3855-3)

Marketing

Marketing Status
Marketed Since 2025-05-30
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": "365e27d8-b610-c19e-e063-6394a90a3610", "openfda": {"upc": ["0368071385533"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["365e1c5c-01b2-bf4e-e063-6394a90a0e43"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3855-3)", "package_ndc": "68071-3855-3", "marketing_start_date": "20250530"}], "brand_name": "Montelukast", "product_id": "68071-3855_365e27d8-b610-c19e-e063-6394a90a3610", "dosage_form": "TABLET", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "68071-3855", "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": "20140911", "listing_expiration_date": "20261231"}