acetazolamide
Generic: acetazolamide
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
acetazolamide
Generic Name
acetazolamide
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetazolamide 125 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-238
Product ID
72789-238_47a93421-8c8c-37aa-e063-6394a90a039c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211556
Listing Expiration
2027-12-31
Marketing Start
2020-01-30
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789238
Hyphenated Format
72789-238
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ANDA211556 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 125 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (72789-238-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47a93421-8c8c-37aa-e063-6394a90a039c", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "upc": ["0372789238012", "0372789237015"], "unii": ["O3FX965V0I"], "rxcui": ["197303", "197304"], "spl_set_id": ["c525ef20-ec9a-4ffd-b5ea-e53c186fe716"], "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": "100 TABLET in 1 BOTTLE, PLASTIC (72789-238-01)", "package_ndc": "72789-238-01", "marketing_start_date": "20220310"}], "brand_name": "Acetazolamide", "product_id": "72789-238_47a93421-8c8c-37aa-e063-6394a90a039c", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "72789-238", "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": "ANDA211556", "marketing_category": "ANDA", "marketing_start_date": "20200130", "listing_expiration_date": "20271231"}