NDC 31722-133 – Potassium Chloride

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

Human Prescription Drug

Product NDC31722-133

Product details

Brand name
Potassium Chloride
Generic name
Potassium CHLORIDE
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA214422
Marketed since
January 20, 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
31722-133-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-01)Jan 20, 2021
31722-133-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-05)Jan 20, 2021

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