Package 71610-563-30

Brand: montelukast

Generic: montelukast
NDC Package

Package Facts

Identity

Package NDC 71610-563-30
Digits Only 7161056330
Product NDC 71610-563
Product ID 71610-563_c18bda87-c173-4af7-9517-43568b1b2727
Description

30 TABLET, FILM COATED in 1 BOTTLE (71610-563-30)

Marketing

Marketing Status
Marketed Since 2021-05-27
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": "c18bda87-c173-4af7-9517-43568b1b2727", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["4fe3c0d4-94ff-43ca-9d24-54676fe593fe"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-563-30)", "package_ndc": "71610-563-30", "marketing_start_date": "20210527"}], "brand_name": "Montelukast", "product_id": "71610-563_c18bda87-c173-4af7-9517-43568b1b2727", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "71610-563", "generic_name": "Montelukast", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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": "20210211", "listing_expiration_date": "20261231"}