NDC 50090-7639 – Potassium Chloride

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

Human Prescription Drug

Product NDC50090-7639

Product details

Brand name
Potassium Chloride
Generic name
Potassium Chloride
Labeler
A-S Medication Solutions
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 (4)

Package NDCDescriptionSince
50090-7639-030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-0)Aug 26, 2025
50090-7639-1100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-1)Aug 26, 2025
50090-7639-290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-2)Aug 26, 2025
50090-7639-360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-3)Aug 26, 2025

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