MedPath

Quinidine Gluconate

QUINIDINE GLUCONATEEXTENDED-RELEASE TABLETS USP

Approved
Approval ID

3af30c3b-944e-4293-baa5-38965b1d1137

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 4, 2016

Manufacturers
FDA

Carilion Materials Management

DUNS: 079239644

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Quinidine Gluconate

PRODUCT DETAILS

NDC Product Code68151-2701
Application NumberANDA089338
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateFebruary 13, 2015
Generic NameQuinidine Gluconate

INGREDIENTS (1)

QUINIDINE GLUCONATEActive
Quantity: 324 mg in 1 1
Code: R6875N380F
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Quinidine Gluconate - FDA Drug Approval Details