DARANIDE

Product NDC

51672-4144

11-digit product format

516724144

Labeler code

51672

Product ID

51672-4144_56dd77b4-82ca-4556-a3d6-fc0d1e88ca29

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

dichlorphenamide

Dosage form

TABLET

Route

ORAL

Labeler

Taro Pharmaceuticals U.S.A., Inc.

Application

NDA011366

Marketing category

NDA

Marketing start

2012-03-16

Marketing end

0000-00-00

Substance

DICHLORPHENAMIDE

Active strength

50 mg/1

Pharmacologic classes

Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [CS],Carbonic Anhydrase Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record