Package 72162-1754-1

Brand: methazolamide

Generic: methazolamide
NDC Package

Package Facts

Identity

Package NDC 72162-1754-1
Digits Only 7216217541
Product NDC 72162-1754
Description

100 TABLET in 1 BOTTLE (72162-1754-1)

Marketing

Marketing Status
Marketed Since 2024-02-05
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": "270d0052-a3fd-4fb2-a168-40c928384cc9", "openfda": {"unii": ["W733B0S9SD"], "rxcui": ["197939"], "spl_set_id": ["504b695a-ac9e-4c71-8755-d31f1958a71c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1754-1)", "package_ndc": "72162-1754-1", "marketing_start_date": "20240205"}], "brand_name": "Methazolamide", "product_id": "72162-1754_270d0052-a3fd-4fb2-a168-40c928384cc9", "dosage_form": "TABLET", "product_ndc": "72162-1754", "generic_name": "Methazolamide", "labeler_name": "Bryant Ranch Prepack", "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"}