acetazolamide

Generic: acetazolamide

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetazolamide
Generic Name acetazolamide
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

acetazolamide sodium 500 mg/5mL

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-831
Product ID 23155-831_8c831077-24e8-4443-bd1d-d8649d1e4257
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202693
Listing Expiration 2026-12-31
Marketing Start 2022-11-15

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 23155831
Hyphenated Format 23155-831

Supplemental Identifiers

RxCUI
307702
UPC
0323155831313
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 ANDA202693 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/5mL
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (23155-831-31) / 5 mL in 1 VIAL, GLASS
source: ndc

Packages (1)

Ingredients (1)

acetazolamide sodium (500 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "8c831077-24e8-4443-bd1d-d8649d1e4257", "openfda": {"upc": ["0323155831313"], "unii": ["429ZT169UH"], "rxcui": ["307702"], "spl_set_id": ["4dd56001-4941-4ff0-9f30-02a1bcc4fe7e"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (23155-831-31)  / 5 mL in 1 VIAL, GLASS", "package_ndc": "23155-831-31", "marketing_start_date": "20221115"}], "brand_name": "Acetazolamide", "product_id": "23155-831_8c831077-24e8-4443-bd1d-d8649d1e4257", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "23155-831", "generic_name": "Acetazolamide", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetazolamide", "active_ingredients": [{"name": "ACETAZOLAMIDE SODIUM", "strength": "500 mg/5mL"}], "application_number": "ANDA202693", "marketing_category": "ANDA", "marketing_start_date": "20221115", "listing_expiration_date": "20261231"}