NDC 68001-396 – Potassium Chloride

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

Human Prescription Drug 1 recall

Product NDC68001-396

Product details

Brand name
Potassium Chloride
Generic name
Potassium Chloride
Labeler
BluePoint Laboratories
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202868
Marketed since
July 3, 2019
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
68001-396-00100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68001-396-00)Jul 3, 2019
68001-396-03500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68001-396-03)Jul 3, 2019

Recalls mentioning this NDC

Other Potassium Chloride products