acetazolamide

Generic: acetazolamide

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetazolamide
Generic Name acetazolamide
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetazolamide 250 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6663
Product ID 0904-6663_33b51d34-f1ed-4c10-ba8c-72e5e37d1d67
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205530
Listing Expiration 2026-12-31
Marketing Start 2013-03-15

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 09046663
Hyphenated Format 0904-6663

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 ANDA205530 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-6663-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-6663-61 100 BLISTER PACK in 1 CARTON (0904-6663-61) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

acetazolamide (250 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": "33b51d34-f1ed-4c10-ba8c-72e5e37d1d67", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "unii": ["O3FX965V0I"], "rxcui": ["197304"], "spl_set_id": ["37135ba5-63fd-427f-9b4a-8b7d1009bbca"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6663-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6663-61", "marketing_start_date": "20130315"}], "brand_name": "acetazolamide", "product_id": "0904-6663_33b51d34-f1ed-4c10-ba8c-72e5e37d1d67", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "0904-6663", "generic_name": "acetazolamide", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "acetazolamide", "active_ingredients": [{"name": "ACETAZOLAMIDE", "strength": "250 mg/1"}], "application_number": "ANDA205530", "marketing_category": "ANDA", "marketing_start_date": "20130315", "listing_expiration_date": "20261231"}