Package 72162-1755-1

Brand: methazolamide

Generic: methazolamide
NDC Package

Package Facts

Identity

Package NDC 72162-1755-1
Digits Only 7216217551
Product NDC 72162-1755
Product ID 72162-1755_6f0f34a3-5b3b-490c-8acc-82e0f433827b
Description

100 TABLET in 1 BOTTLE (72162-1755-1)

Marketing

Marketing Status
Marketed Since 2024-02-05
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": "6f0f34a3-5b3b-490c-8acc-82e0f433827b", "openfda": {"unii": ["W733B0S9SD"], "rxcui": ["197940"], "spl_set_id": ["369e89a4-9898-4a9f-a316-17d0fce8a08b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1755-1)", "package_ndc": "72162-1755-1", "marketing_start_date": "20240205"}], "brand_name": "Methazolamide", "product_id": "72162-1755_6f0f34a3-5b3b-490c-8acc-82e0f433827b", "dosage_form": "TABLET", "product_ndc": "72162-1755", "generic_name": "Methazolamide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methazolamide", "active_ingredients": [{"name": "METHAZOLAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA040001", "marketing_category": "ANDA", "marketing_start_date": "20141106", "listing_expiration_date": "20261231"}