acetazolamide
Generic: acetazolamide
Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.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
Active Ingredients
acetazolamide sodium 500 mg/5mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
23155831
Hyphenated Format
23155-831
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
acetazolamide (source: ndc)
Generic Name
acetazolamide (source: ndc)
Application Number
ANDA202693 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/5mL
Packaging
- 1 VIAL, GLASS in 1 CARTON (23155-831-31) / 5 mL in 1 VIAL, GLASS
Packages (1)
Ingredients (1)
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"}