Methazolamide

Generic: methazolamide

Labeler: Oceanside Pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Methazolamide
Generic Name methazolamide
Labeler Oceanside Pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

METHAZOLAMIDE 50 mg/1

Identifiers & Regulatory

Product NDC 68682-023
Product ID 68682-023_0962cf33-b872-4006-82f8-8610567a07d6
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 68682023
Hyphenated Format 68682-023

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 (68682-023-01)
  • 100 TABLET in 1 BOTTLE (68682-023-10)
  • 500 TABLET in 1 BOTTLE (68682-023-50)
  • 90 TABLET in 1 BOTTLE (68682-023-90)
source: ndc

Packages (4)

68682-023-01 1000 TABLET in 1 BOTTLE (68682-023-01) 68682-023-10 100 TABLET in 1 BOTTLE (68682-023-10) 68682-023-50 500 TABLET in 1 BOTTLE (68682-023-50) 68682-023-90 90 TABLET in 1 BOTTLE (68682-023-90)

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": "0962cf33-b872-4006-82f8-8610567a07d6", "openfda": {"upc": ["0368682023107", "0368682022100"], "unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["0962cf33-b872-4006-82f8-8610567a07d6"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (68682-023-01)", "package_ndc": "68682-023-01", "marketing_start_date": "20201002"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (68682-023-10)", "package_ndc": "68682-023-10", "marketing_start_date": "20201002"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68682-023-50)", "package_ndc": "68682-023-50", "marketing_start_date": "20201002"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68682-023-90)", "package_ndc": "68682-023-90", "marketing_start_date": "20201002"}], "brand_name": "Methazolamide", "product_id": "68682-023_0962cf33-b872-4006-82f8-8610567a07d6", "dosage_form": "TABLET", "product_ndc": "68682-023", "generic_name": "methazolamide", "labeler_name": "Oceanside Pharmaceuticals", "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"}