methazolamide

Generic: methazolamide

Labeler: padagis us llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methazolamide
Generic Name methazolamide
Labeler padagis us llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methazolamide 50 mg/1

Manufacturer
Padagis US LLC

Identifiers & Regulatory

Product NDC 0574-0791
Product ID 0574-0791_94b58ed4-5a45-4777-924c-7608156be1b0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040062
Marketing Start 2014-09-30
Marketing End 2027-09-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05740791
Hyphenated Format 0574-0791

Supplemental Identifiers

RxCUI
197939 197940
UPC
0305740790014 0305740791011
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 ANDA040062 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (0574-0791-01)
source: ndc

Packages (1)

0574-0791-01 100 TABLET in 1 BOTTLE, PLASTIC (0574-0791-01)

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": "94b58ed4-5a45-4777-924c-7608156be1b0", "openfda": {"upc": ["0305740790014", "0305740791011"], "unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["5e0795e1-d5c5-4b04-9bce-077bb8028023"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0574-0791-01)", "package_ndc": "0574-0791-01", "marketing_end_date": "20260831", "marketing_start_date": "20140930"}], "brand_name": "methazolamide", "product_id": "0574-0791_94b58ed4-5a45-4777-924c-7608156be1b0", "dosage_form": "TABLET", "product_ndc": "0574-0791", "generic_name": "methazolamide", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "methazolamide", "active_ingredients": [{"name": "METHAZOLAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA040062", "marketing_category": "ANDA", "marketing_end_date": "20270930", "marketing_start_date": "20140930"}