acetazolamide

Generic: acetazolamide

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetazolamide
Generic Name acetazolamide
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

acetazolamide sodium 500 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9006
Product ID 0143-9006_6468455a-a638-4ef0-8bce-41afa7f24c66
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040089
Listing Expiration 2026-12-31
Marketing Start 1996-05-01

Pharmacologic Class

Classes
carbonic anhydrase inhibitor [epc] carbonic anhydrase inhibitors [moa] sulfonamides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439006
Hyphenated Format 0143-9006

Supplemental Identifiers

RxCUI
307702
UNII
429ZT169UH

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 acetazolamide (source: ndc)
Generic Name acetazolamide (source: ndc)
Application Number ANDA040089 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (0143-9006-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

0143-9006-01 1 VIAL in 1 CARTON (0143-9006-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Ingredients (1)

acetazolamide sodium (500 mg/1)

Linked Drug Pages (1)

AcetaZOLAMIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "6468455a-a638-4ef0-8bce-41afa7f24c66", "openfda": {"unii": ["429ZT169UH"], "rxcui": ["307702"], "spl_set_id": ["5502e5ba-9b5e-460a-855f-60534b625461"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0143-9006-01)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "0143-9006-01", "marketing_start_date": "19960501"}], "brand_name": "AcetaZOLAMIDE", "product_id": "0143-9006_6468455a-a638-4ef0-8bce-41afa7f24c66", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "0143-9006", "generic_name": "Acetazolamide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AcetaZOLAMIDE", "active_ingredients": [{"name": "ACETAZOLAMIDE SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA040089", "marketing_category": "ANDA", "marketing_start_date": "19960501", "listing_expiration_date": "20261231"}