Package 0574-0791-01

Brand: methazolamide

Generic: methazolamide
NDC Package

Package Facts

Identity

Package NDC 0574-0791-01
Digits Only 0574079101
Product NDC 0574-0791
Product ID 0574-0791_94b58ed4-5a45-4777-924c-7608156be1b0
Description

100 TABLET in 1 BOTTLE, PLASTIC (0574-0791-01)

Marketing

Marketing Status
Discontinued 2026-08-31
Brand methazolamide
Generic methazolamide
Sample Package No

Linked Drug Pages (1)

methazolamide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "94b58ed4-5a45-4777-924c-7608156be1b0", "openfda": {"upc": ["0305740790014", "0305740791011"], "unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["5e0795e1-d5c5-4b04-9bce-077bb8028023"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0574-0791-01)", "package_ndc": "0574-0791-01", "marketing_end_date": "20260831", "marketing_start_date": "20140930"}], "brand_name": "methazolamide", "product_id": "0574-0791_94b58ed4-5a45-4777-924c-7608156be1b0", "dosage_form": "TABLET", "product_ndc": "0574-0791", "generic_name": "methazolamide", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "methazolamide", "active_ingredients": [{"name": "METHAZOLAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA040062", "marketing_category": "ANDA", "marketing_end_date": "20270930", "marketing_start_date": "20140930"}