acetazolamide

Generic: acetazolamide

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetazolamide
Generic Name acetazolamide
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetazolamide 250 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7536
Product ID 50090-7536_0c0d69e8-f78e-4286-ad4a-77e3719e16ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211069
Listing Expiration 2027-12-31
Marketing Start 2023-07-15

Pharmacologic Class

Established (EPC)
carbonic anhydrase inhibitor [epc]
Mechanism of Action
carbonic anhydrase inhibitors [moa]
Chemical Structure
sulfonamides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907536
Hyphenated Format 50090-7536

Supplemental Identifiers

RxCUI
197304
UNII
O3FX965V0I
NUI
N0000175517 N0000000235 M0020790

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 acetazolamide (source: ndc)
Generic Name acetazolamide (source: ndc)
Application Number ANDA211069 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 12 TABLET in 1 BOTTLE (50090-7536-0)
source: ndc

Packages (1)

50090-7536-0 12 TABLET in 1 BOTTLE (50090-7536-0)

Ingredients (1)

acetazolamide (250 mg/1)

Linked Drug Pages (1)

acetaZOLAMIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0c0d69e8-f78e-4286-ad4a-77e3719e16ac", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "unii": ["O3FX965V0I"], "rxcui": ["197304"], "spl_set_id": ["b339843f-0324-4996-88a0-0619fd6f867b"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (50090-7536-0)", "package_ndc": "50090-7536-0", "marketing_start_date": "20250409"}], "brand_name": "acetaZOLAMIDE", "product_id": "50090-7536_0c0d69e8-f78e-4286-ad4a-77e3719e16ac", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "50090-7536", "generic_name": "acetaZOLAMIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "acetaZOLAMIDE", "active_ingredients": [{"name": "ACETAZOLAMIDE", "strength": "250 mg/1"}], "application_number": "ANDA211069", "marketing_category": "ANDA", "marketing_start_date": "20230715", "listing_expiration_date": "20271231"}