methazolamide

Generic: methazolamide

Labeler: bausch & lomb incorporated
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methazolamide
Generic Name methazolamide
Labeler bausch & lomb incorporated
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methazolamide 50 mg/1

Manufacturer
Bausch & Lomb Incorporated

Identifiers & Regulatory

Product NDC 24208-023
Product ID 24208-023_41d745af-7d7b-dc08-e063-6394a90a2fbf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207438
Listing Expiration 2026-12-31
Marketing Start 2020-10-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24208023
Hyphenated Format 24208-023

Supplemental Identifiers

RxCUI
197939 197940
UPC
0324208022108 0324208023105
UNII
W733B0S9SD

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name methazolamide (source: ndc)
Generic Name methazolamide (source: ndc)
Application Number ANDA207438 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (24208-023-01)
  • 100 TABLET in 1 BOTTLE (24208-023-10)
  • 500 TABLET in 1 BOTTLE (24208-023-50)
  • 90 TABLET in 1 BOTTLE (24208-023-90)
source: ndc

Packages (4)

24208-023-01 1000 TABLET in 1 BOTTLE (24208-023-01) 24208-023-10 100 TABLET in 1 BOTTLE (24208-023-10) 24208-023-50 500 TABLET in 1 BOTTLE (24208-023-50) 24208-023-90 90 TABLET in 1 BOTTLE (24208-023-90)

Ingredients (1)

methazolamide (50 mg/1)

Linked Drug Pages (1)

Methazolamide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41d745af-7d7b-dc08-e063-6394a90a2fbf", "openfda": {"upc": ["0324208022108", "0324208023105"], "unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["0c0ba5c7-c53e-4e29-a7ff-48fddc5a9258"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (24208-023-01)", "package_ndc": "24208-023-01", "marketing_start_date": "20201002"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (24208-023-10)", "package_ndc": "24208-023-10", "marketing_start_date": "20201002"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (24208-023-50)", "package_ndc": "24208-023-50", "marketing_start_date": "20201002"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (24208-023-90)", "package_ndc": "24208-023-90", "marketing_start_date": "20201002"}], "brand_name": "Methazolamide", "product_id": "24208-023_41d745af-7d7b-dc08-e063-6394a90a2fbf", "dosage_form": "TABLET", "product_ndc": "24208-023", "generic_name": "methazolamide", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methazolamide", "active_ingredients": [{"name": "METHAZOLAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA207438", "marketing_category": "ANDA", "marketing_start_date": "20201002", "listing_expiration_date": "20261231"}