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 TABLET
Routes
ORAL
Active Ingredients

acetazolamide 125 mg/1

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

Identifiers & Regulatory

Product NDC 23155-287
Product ID 23155-287_a68d90ee-c8ca-4f10-94a5-6259c4922d48
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205530
Listing Expiration 2027-12-31
Marketing Start 2016-10-27

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 23155287
Hyphenated Format 23155-287

Supplemental Identifiers

RxCUI
197303 197304
UPC
0323155288018 0323155288100 0323155287011 0323155287103
UNII
O3FX965V0I
NUI
N0000175517 N0000000235 M0020790

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 ANDA205530 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-287-01)
  • 1000 TABLET in 1 BOTTLE (23155-287-10)
source: ndc

Packages (2)

23155-287-01 100 TABLET in 1 BOTTLE (23155-287-01) 23155-287-10 1000 TABLET in 1 BOTTLE (23155-287-10)

Ingredients (1)

acetazolamide (125 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": "a68d90ee-c8ca-4f10-94a5-6259c4922d48", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "upc": ["0323155288018", "0323155288100", "0323155287011", "0323155287103"], "unii": ["O3FX965V0I"], "rxcui": ["197303", "197304"], "spl_set_id": ["0700a910-79aa-4431-aecf-637fe14fcae8"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-287-01)", "package_ndc": "23155-287-01", "marketing_start_date": "20161027"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-287-10)", "package_ndc": "23155-287-10", "marketing_start_date": "20161027"}], "brand_name": "acetazolamide", "product_id": "23155-287_a68d90ee-c8ca-4f10-94a5-6259c4922d48", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "23155-287", "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", "strength": "125 mg/1"}], "application_number": "ANDA205530", "marketing_category": "ANDA", "marketing_start_date": "20161027", "listing_expiration_date": "20271231"}