acetazolamide

Generic: acetazolamide

Labeler: nucare pharmaceuticlas, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetazolamide
Generic Name acetazolamide
Labeler nucare pharmaceuticlas, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetazolamide 125 mg/1

Manufacturer
NuCare Pharmaceuticlas, Inc.

Identifiers & Regulatory

Product NDC 68071-3728
Product ID 68071-3728_27888b41-786a-8b5f-e063-6394a90adb98
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209734
Listing Expiration 2026-12-31
Marketing Start 2017-11-20

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 680713728
Hyphenated Format 68071-3728

Supplemental Identifiers

RxCUI
197303
UPC
0368071372816
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 ANDA209734 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/1
source: ndc
Packaging
  • 12 TABLET in 1 BOTTLE (68071-3728-1)
source: ndc

Packages (1)

68071-3728-1 12 TABLET in 1 BOTTLE (68071-3728-1)

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": "27888b41-786a-8b5f-e063-6394a90adb98", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "upc": ["0368071372816"], "unii": ["O3FX965V0I"], "rxcui": ["197303"], "spl_set_id": ["278878bc-da9c-09d4-e063-6394a90abaf7"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticlas, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (68071-3728-1)", "package_ndc": "68071-3728-1", "marketing_start_date": "20241122"}], "brand_name": "Acetazolamide", "product_id": "68071-3728_27888b41-786a-8b5f-e063-6394a90adb98", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "68071-3728", "generic_name": "Acetazolamide", "labeler_name": "NuCare Pharmaceuticlas, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetazolamide", "active_ingredients": [{"name": "ACETAZOLAMIDE", "strength": "125 mg/1"}], "application_number": "ANDA209734", "marketing_category": "ANDA", "marketing_start_date": "20171120", "listing_expiration_date": "20261231"}