methazolamide

Generic: methazolamide

Labeler: precision dose, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methazolamide
Generic Name methazolamide
Labeler precision dose, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methazolamide 50 mg/1

Manufacturer
Precision Dose, Inc.

Identifiers & Regulatory

Product NDC 68094-808
Product ID 68094-808_5dc8c6ca-5710-4369-b0ae-37666210f03b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215615
Listing Expiration 2026-12-31
Marketing Start 2023-11-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68094808
Hyphenated Format 68094-808

Supplemental Identifiers

RxCUI
197939 197940
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 ANDA215615 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68094-808-50)
source: ndc

Packages (1)

68094-808-50 100 TABLET in 1 BOTTLE (68094-808-50)

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": "5dc8c6ca-5710-4369-b0ae-37666210f03b", "openfda": {"unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["1e0e81c7-a328-4034-a6b3-4c83e9ac3a3e"], "manufacturer_name": ["Precision Dose, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68094-808-50)", "package_ndc": "68094-808-50", "marketing_start_date": "20231130"}], "brand_name": "Methazolamide", "product_id": "68094-808_5dc8c6ca-5710-4369-b0ae-37666210f03b", "dosage_form": "TABLET", "product_ndc": "68094-808", "generic_name": "Methazolamide", "labeler_name": "Precision Dose, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methazolamide", "active_ingredients": [{"name": "METHAZOLAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA215615", "marketing_category": "ANDA", "marketing_start_date": "20231130", "listing_expiration_date": "20261231"}