Package 50090-6109-0

Brand: montelukast

Generic: montelukast
NDC Package

Package Facts

Identity

Package NDC 50090-6109-0
Digits Only 5009061090
Product NDC 50090-6109
Product ID 50090-6109_b1ddd118-1dcd-475c-986b-20a2c1536eaf
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6109-0)

Marketing

Marketing Status
Marketed Since 2022-09-28
Brand montelukast
Generic montelukast
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b1ddd118-1dcd-475c-986b-20a2c1536eaf", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["da9821f1-536a-416b-9594-210bde0cefaf"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6109-0)", "package_ndc": "50090-6109-0", "marketing_start_date": "20220928"}], "brand_name": "Montelukast", "product_id": "50090-6109_b1ddd118-1dcd-475c-986b-20a2c1536eaf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "50090-6109", "generic_name": "Montelukast", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA202843", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20261231"}