NDC 72065-001

Keveyis

Dichlorphenamide

Keveyis is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Xeris Pharmaceuticals, Inc.. The primary component is Dichlorphenamide.

• Product ID: 72065-001_d30a8795-39d2-51c3-e053-2995a90abcf0
• NDC: 72065-001
• Product Type: Human Prescription Drug
• Proprietary Name: Keveyis
• Generic Name: Dichlorphenamide
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2021-12-13
• Marketing Category: NDA /
• Application Number: NDA011366
• Labeler Name: Xeris Pharmaceuticals, Inc.
• Substance Name: DICHLORPHENAMIDE
• Active Ingredient Strength: 50 mg/1
• Pharm Classes: Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [CS],Carbonic Anhydrase Inhibitor [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 72065-001-01

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

• Marketing Start Date: 2021-12-13
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Keveyis" or generic name "Dichlorphenamide"

NDC	Brand Name	Generic Name
51672-4177	Keveyis	Dichlorphenamide
71090-001	Keveyis	Dichlorphenamide
72065-001	Keveyis	Dichlorphenamide
51672-4144	DARANIDE	dichlorphenamide
13668-676	Dichlorphenamide	Dichlorphenamide