Package 50268-556-15

Brand: montelukast

Generic: montelukast
NDC Package

Package Facts

Identity

Package NDC 50268-556-15
Digits Only 5026855615
Product NDC 50268-556
Product ID 50268-556_47e755f4-d852-60b7-e063-6294a90aa1e4
Description

50 BLISTER PACK in 1 BOX (50268-556-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-556-11)

Marketing

Marketing Status
Marketed Since 2022-02-08
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": "47e755f4-d852-60b7-e063-6294a90aa1e4", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["d7870c45-5a8b-8369-e053-2a95a90ae1f3"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-556-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-556-11)", "package_ndc": "50268-556-15", "marketing_start_date": "20220208"}], "brand_name": "Montelukast", "product_id": "50268-556_47e755f4-d852-60b7-e063-6294a90aa1e4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "50268-556", "generic_name": "Montelukast", "labeler_name": "AvPAK", "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": "20220208", "listing_expiration_date": "20271231"}