NDC 68001-518 – Potassium Chloride

Potassium Chloride 750 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC68001-518

Product details

Brand name
Potassium Chloride
Generic name
Potassium Chloride
Labeler
BluePoint Laboratories
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210921
Marketed since
September 10, 2021
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
68001-518-00100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-00)Sep 10, 2021
68001-518-081000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-08)Sep 10, 2021

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