keveyis

Generic: dichlorphenamide

Labeler: xeris pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name keveyis
Generic Name dichlorphenamide
Labeler xeris pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dichlorphenamide 50 mg/1

Manufacturer
Xeris Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72065-001
Product ID 72065-001_1a581a6b-8813-42ed-8892-21c2341b62c0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA011366
Listing Expiration 2027-12-31
Marketing Start 2021-12-13

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 72065001
Hyphenated Format 72065-001

Supplemental Identifiers

RxCUI
197594 1661799
UPC
0372065001019
UNII
VVJ6673MHY
NUI
N0000175517 N0000000235 M0020790

Packaging Origin

Original Packager
true

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 keveyis (source: ndc)
Generic Name dichlorphenamide (source: ndc)
Application Number NDA011366 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72065-001-01)
source: ndc

Packages (1)

72065-001-01 100 TABLET in 1 BOTTLE (72065-001-01)

Ingredients (1)

dichlorphenamide (50 mg/1)

Linked Drug Pages (1)

Keveyis ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1a581a6b-8813-42ed-8892-21c2341b62c0", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "upc": ["0372065001019"], "unii": ["VVJ6673MHY"], "rxcui": ["197594", "1661799"], "spl_set_id": ["d30a87b9-90fb-35b2-e053-2995a90aea2c"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["Xeris Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72065-001-01)", "package_ndc": "72065-001-01", "marketing_start_date": "20211213"}], "brand_name": "Keveyis", "product_id": "72065-001_1a581a6b-8813-42ed-8892-21c2341b62c0", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "72065-001", "generic_name": "Dichlorphenamide", "labeler_name": "Xeris Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Keveyis", "active_ingredients": [{"name": "DICHLORPHENAMIDE", "strength": "50 mg/1"}], "application_number": "NDA011366", "marketing_category": "NDA", "marketing_start_date": "20211213", "listing_expiration_date": "20271231"}