NDC 0591-2682 – Potassium Citrate

Potassium Citrate 5 meq/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC0591-2682

Product details

Brand name
Potassium Citrate
Generic name
Potassium Citrate
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA209758
Marketed since
May 30, 2018
Marketing end
June 30, 2027
Pharmacologic class
Anti-coagulant; Calculi Dissolution Agent

Active ingredients

Uses, dosage, side effects and warnings for Potassium Citrate →

Package NDC codes (1)

Package NDCDescriptionSince
0591-2682-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0591-2682-01)May 30, 2018

Other Potassium Citrate products