Package 42571-239-90

Brand: methazolamide

Generic: methazolamide
NDC Package

Package Facts

Identity

Package NDC 42571-239-90
Digits Only 4257123990
Product NDC 42571-239
Description

90 TABLET in 1 BOTTLE (42571-239-90)

Marketing

Marketing Status
Marketed Since 2019-03-05
Brand methazolamide
Generic methazolamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9ebf7533-27e6-54c2-e053-2995a90ae560", "openfda": {"upc": ["0342571239909", "0342571240905"], "unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["91a493f5-f8c3-4b64-a15e-b550d8631668"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (42571-239-05)", "package_ndc": "42571-239-05", "marketing_start_date": "20190305"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42571-239-10)", "package_ndc": "42571-239-10", "marketing_start_date": "20190305"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42571-239-90)", "package_ndc": "42571-239-90", "marketing_start_date": "20190305"}], "brand_name": "METHAZOLAMIDE", "product_id": "42571-239_9ebf7533-27e6-54c2-e053-2995a90ae560", "dosage_form": "TABLET", "product_ndc": "42571-239", "generic_name": "Methazolamide", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHAZOLAMIDE", "active_ingredients": [{"name": "METHAZOLAMIDE", "strength": "25 mg/1"}], "application_number": "ANDA207438", "marketing_category": "ANDA", "marketing_start_date": "20190305", "listing_expiration_date": "20261231"}