Package 16571-100-10

Brand: montelukast sodium

Generic: montelukast sodium
NDC Package

Package Facts

Identity

Package NDC 16571-100-10
Digits Only 1657110010
Product NDC 16571-100
Description

1000 TABLET in 1 BOTTLE (16571-100-10)

Marketing

Marketing Status
Marketed Since 2023-06-01
Brand montelukast sodium
Generic montelukast sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c3c93ca9-9367-4426-b310-5507dd588b08", "openfda": {"upc": ["0316571100095"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["75723c5a-3c9e-468a-bc65-57b4c755889a"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (16571-100-09)", "package_ndc": "16571-100-09", "marketing_start_date": "20230601"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16571-100-10)", "package_ndc": "16571-100-10", "marketing_start_date": "20230601"}], "brand_name": "MONTELUKAST SODIUM", "product_id": "16571-100_c3c93ca9-9367-4426-b310-5507dd588b08", "dosage_form": "TABLET", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "16571-100", "generic_name": "MONTELUKAST SODIUM", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MONTELUKAST SODIUM", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA209012", "marketing_category": "ANDA", "marketing_start_date": "20230601", "listing_expiration_date": "20261231"}