methazolamide

Generic: methazolamide

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methazolamide
Generic Name methazolamide
Labeler ani pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methazolamide 25 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 62559-240
Product ID 62559-240_7a4099f0-7e1b-49ae-ae13-1463c08daaa5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040001
Listing Expiration 2026-12-31
Marketing Start 2014-11-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62559240
Hyphenated Format 62559-240

Supplemental Identifiers

RxCUI
197939 197940
UPC
0362559240017 0362559241014
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 ANDA040001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (62559-240-01)
source: ndc

Packages (1)

62559-240-01 100 TABLET in 1 BOTTLE (62559-240-01)

Ingredients (1)

methazolamide (25 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": "7a4099f0-7e1b-49ae-ae13-1463c08daaa5", "openfda": {"upc": ["0362559240017", "0362559241014"], "unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["c26c8834-961e-4c9c-9ad4-5db2d9419938"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62559-240-01)", "package_ndc": "62559-240-01", "marketing_start_date": "20141106"}], "brand_name": "Methazolamide", "product_id": "62559-240_7a4099f0-7e1b-49ae-ae13-1463c08daaa5", "dosage_form": "TABLET", "product_ndc": "62559-240", "generic_name": "Methazolamide", "labeler_name": "ANI Pharmaceuticals, Inc.", "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"}