Package 62559-240-01

Brand: methazolamide

Generic: methazolamide
NDC Package

Package Facts

Identity

Package NDC 62559-240-01
Digits Only 6255924001
Product NDC 62559-240
Description

100 TABLET in 1 BOTTLE (62559-240-01)

Marketing

Marketing Status
Marketed Since 2014-11-06
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": "7a4099f0-7e1b-49ae-ae13-1463c08daaa5", "openfda": {"upc": ["0362559240017", "0362559241014"], "unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["c26c8834-961e-4c9c-9ad4-5db2d9419938"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62559-240-01)", "package_ndc": "62559-240-01", "marketing_start_date": "20141106"}], "brand_name": "Methazolamide", "product_id": "62559-240_7a4099f0-7e1b-49ae-ae13-1463c08daaa5", "dosage_form": "TABLET", "product_ndc": "62559-240", "generic_name": "Methazolamide", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methazolamide", "active_ingredients": [{"name": "METHAZOLAMIDE", "strength": "25 mg/1"}], "application_number": "ANDA040001", "marketing_category": "ANDA", "marketing_start_date": "20141106", "listing_expiration_date": "20261231"}