acetazolamide

Generic: acetazolamide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetazolamide
Generic Name acetazolamide
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetazolamide 250 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1979
Product ID 72162-1979_7fe7b6cf-d273-44b7-bb5c-8ce3fe6d7690
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214282
Listing Expiration 2026-12-31
Marketing Start 2020-11-13

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 721621979
Hyphenated Format 72162-1979

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 ANDA214282 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-1979-1)
source: ndc

Packages (1)

Ingredients (1)

acetazolamide (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7fe7b6cf-d273-44b7-bb5c-8ce3fe6d7690", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "unii": ["O3FX965V0I"], "rxcui": ["197304"], "spl_set_id": ["84a582a9-c7e5-4159-a5eb-a47a96b4afc0"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1979-1)", "package_ndc": "72162-1979-1", "marketing_start_date": "20201113"}], "brand_name": "Acetazolamide", "product_id": "72162-1979_7fe7b6cf-d273-44b7-bb5c-8ce3fe6d7690", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "72162-1979", "generic_name": "Acetazolamide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetazolamide", "active_ingredients": [{"name": "ACETAZOLAMIDE", "strength": "250 mg/1"}], "application_number": "ANDA214282", "marketing_category": "ANDA", "marketing_start_date": "20201113", "listing_expiration_date": "20261231"}