methazolamide

Generic: methazolamide

Labeler: micro labs limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methazolamide
Generic Name methazolamide
Labeler micro labs limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methazolamide 50 mg/1

Manufacturer
Micro Labs Limited

Identifiers & Regulatory

Product NDC 42571-240
Product ID 42571-240_9ebf7533-27e6-54c2-e053-2995a90ae560
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207438
Listing Expiration 2026-12-31
Marketing Start 2019-03-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42571240
Hyphenated Format 42571-240

Supplemental Identifiers

RxCUI
197939 197940
UPC
0342571239909 0342571240905
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
  • 500 TABLET in 1 BOTTLE (42571-240-05)
  • 1000 TABLET in 1 BOTTLE (42571-240-10)
  • 90 TABLET in 1 BOTTLE (42571-240-90)
source: ndc

Packages (3)

42571-240-05 500 TABLET in 1 BOTTLE (42571-240-05) 42571-240-10 1000 TABLET in 1 BOTTLE (42571-240-10) 42571-240-90 90 TABLET in 1 BOTTLE (42571-240-90)

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": "9ebf7533-27e6-54c2-e053-2995a90ae560", "openfda": {"upc": ["0342571239909", "0342571240905"], "unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["91a493f5-f8c3-4b64-a15e-b550d8631668"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (42571-240-05)", "package_ndc": "42571-240-05", "marketing_start_date": "20190305"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42571-240-10)", "package_ndc": "42571-240-10", "marketing_start_date": "20190305"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42571-240-90)", "package_ndc": "42571-240-90", "marketing_start_date": "20190305"}], "brand_name": "METHAZOLAMIDE", "product_id": "42571-240_9ebf7533-27e6-54c2-e053-2995a90ae560", "dosage_form": "TABLET", "product_ndc": "42571-240", "generic_name": "Methazolamide", "labeler_name": "Micro Labs Limited", "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": "20190305", "listing_expiration_date": "20261231"}