acetazolamide

Generic: acetazolamide

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetazolamide
Generic Name acetazolamide
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetazolamide 125 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-045
Product ID 72789-045_4af3a096-3d49-ebc1-e063-6294a90a6892
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209734
Listing Expiration 2027-12-31
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 72789045
Hyphenated Format 72789-045

Supplemental Identifiers

RxCUI
197303
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
  • 6 TABLET in 1 BOTTLE, PLASTIC (72789-045-06)
  • 12 TABLET in 1 BOTTLE, PLASTIC (72789-045-12)
source: ndc

Packages (2)

72789-045-06 6 TABLET in 1 BOTTLE, PLASTIC (72789-045-06) 72789-045-12 12 TABLET in 1 BOTTLE, PLASTIC (72789-045-12)

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": "4af3a096-3d49-ebc1-e063-6294a90a6892", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "unii": ["O3FX965V0I"], "rxcui": ["197303"], "spl_set_id": ["268db224-d5db-457c-86bc-972c9fe07917"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (72789-045-06)", "package_ndc": "72789-045-06", "marketing_start_date": "20210104"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (72789-045-12)", "package_ndc": "72789-045-12", "marketing_start_date": "20210106"}], "brand_name": "Acetazolamide", "product_id": "72789-045_4af3a096-3d49-ebc1-e063-6294a90a6892", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "72789-045", "generic_name": "Acetazolamide", "labeler_name": "PD-Rx Pharmaceuticals, 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": "20271231"}