NDC 0832-5322 – Potassium Chloride

Potassium Chloride 600 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC0832-5322

Product details

Brand name
Potassium Chloride
Generic name
Potassium Chloride
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
NDA · NDA019123
Marketed since
April 17, 1986
Listing expires
December 31, 2026
Pharmacologic class
Osmotic Laxative; Potassium Salt

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0832-5322-101000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5322-10)Jun 21, 2019
0832-5322-11100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5322-11)Jun 21, 2019

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