NDC 53489-141 – Quinidine Gluconate

Quinidine Gluconate 324 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC53489-141

Product details

Brand name
Quinidine Gluconate
Generic name
Quinidine Gluconate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA089338
Marketed since
February 10, 1987
Listing expires
December 31, 2026
Pharmacologic class
Antiarrhythmic; Cytochrome P450 2D6 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Quinidine gluconate →

Package NDC codes (7)

Package NDCDescriptionSince
53489-141-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-01)Feb 10, 1987
53489-141-03250 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-03)Feb 10, 1987
53489-141-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-05)Feb 10, 1987
53489-141-0660 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-06)Feb 10, 1987
53489-141-0730 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-07)Feb 10, 1987
53489-141-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-10)Feb 10, 1987
53489-141-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-90)Feb 10, 1987

Other Quinidine gluconate products