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Medicines · US (FDA)

FDA 1982

Antiarrhythmics, class Ia

Quinidine Gluconate

Approved 29 Sept 1982OralTablet, extended release

The FDA lists this product in 10 strengths and forms.

Official labelAsk Osler about it

On this page

Composition
Strengths and forms
Official product information

The table holds no label text for this product yet, only the facts beside it. The official product information has the full text.

Composition

Active ingredients: QUINIDINE GLUCONATE 324MG

Strengths and forms

The FDA lists each strength of a product separately; these pages share one label.

QUINIDINE GLUCONATE 324MG · Tablet, extended releaseThis page
QUINIDINE GLUCONATE 324MG · Tablet, extended releaseANDA087785-001 · Discontinued
QUINIDINE GLUCONATE 324MG · Tablet, extended releaseANDA089338-001 · Prescription
QUINIDINE GLUCONATE 80MG/ML · InjectableNDA007529-002 · Discontinued
QUINIDINE GLUCONATE 324MG · Tablet, extended releaseANDA089476-001 · Discontinued
QUINIDINE GLUCONATE 324MG · Tablet, extended releaseANDA088431-001 · Discontinued
QUINIDINE GLUCONATE 324MG · Tablet, extended releaseANDA088582-001 · Discontinued
QUINIDINE GLUCONATE 324MG · Tablet, extended releaseANDA089164-001 · Discontinued
QUINIDINE GLUCONATE 324MG · Tablet, extended releaseANDA089894-001 · Discontinued
QUINIDINE GLUCONATE 324MG · Tablet, extended release

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

ANDA212589-001 · Prescription

Official product information

Drugs@FDA lists the approved labels, letters and reviews for application ANDA087810.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Brand name: Quinidine Gluconate
Drug class: Antiarrhythmics, class Ia
Route: Oral
Dosage form: Tablet, extended release
Applicant: Ani Pharms
Status: Discontinued
FDA approval: 29 Sept 1982
Application: ANDA087810-001
RxCUI: 35220