methazolamide
Generic: methazolamide
Labeler: northstar rx llcDrug Facts
Product Profile
Brand Name
methazolamide
Generic Name
methazolamide
Labeler
northstar rx llc
Dosage Form
TABLET
Routes
Active Ingredients
methazolamide 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72603-167
Product ID
72603-167_042586b3-4d4a-c5ae-e063-6394a90aaa7c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040001
Listing Expiration
2026-12-31
Marketing Start
2023-08-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72603167
Hyphenated Format
72603-167
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (72603-167-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "042586b3-4d4a-c5ae-e063-6394a90aaa7c", "openfda": {"upc": ["0372603166019", "0372603167016"], "unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["042586b3-4d49-c5ae-e063-6394a90aaa7c"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-167-01)", "package_ndc": "72603-167-01", "marketing_start_date": "20230830"}], "brand_name": "Methazolamide", "product_id": "72603-167_042586b3-4d4a-c5ae-e063-6394a90aaa7c", "dosage_form": "TABLET", "product_ndc": "72603-167", "generic_name": "Methazolamide", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methazolamide", "active_ingredients": [{"name": "METHAZOLAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA040001", "marketing_category": "ANDA", "marketing_start_date": "20230830", "listing_expiration_date": "20261231"}