Package 72603-166-01

Brand: methazolamide

Generic: methazolamide
NDC Package

Package Facts

Identity

Package NDC 72603-166-01
Digits Only 7260316601
Product NDC 72603-166
Product ID 72603-166_042586b3-4d4a-c5ae-e063-6394a90aaa7c
Description

100 TABLET in 1 BOTTLE (72603-166-01)

Marketing

Marketing Status
Marketed Since 2023-08-30
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": "042586b3-4d4a-c5ae-e063-6394a90aaa7c", "openfda": {"upc": ["0372603166019", "0372603167016"], "unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["042586b3-4d49-c5ae-e063-6394a90aaa7c"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-166-01)", "package_ndc": "72603-166-01", "marketing_start_date": "20230830"}], "brand_name": "Methazolamide", "product_id": "72603-166_042586b3-4d4a-c5ae-e063-6394a90aaa7c", "dosage_form": "TABLET", "product_ndc": "72603-166", "generic_name": "Methazolamide", "labeler_name": "NorthStar Rx LLC", "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": "20230830", "listing_expiration_date": "20261231"}