NDC 68382-537 – Potassium Citrate

Potassium Citrate 10 meq/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC68382-537

Product details

Brand name
Potassium Citrate
Generic name
Potassium Citrate
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203546
Marketed since
August 12, 2014
Listing expires
December 31, 2026
Pharmacologic class
Anti-coagulant; Calculi Dissolution Agent

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
68382-537-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-01)Aug 12, 2014
68382-537-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-05)Aug 12, 2014
68382-537-0630 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-06)Aug 12, 2014
68382-537-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-10)Aug 12, 2014
68382-537-1690 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-16)Aug 12, 2014
68382-537-3010 BLISTER PACK in 1 CARTON (68382-537-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKAug 12, 2014

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