NDC 68462-357 – Potassium Chloride

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

Human Prescription Drug 4 recalls

Product NDC68462-357

Product details

Brand name
Potassium Chloride
Generic name
Potassium Chloride
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202868
Marketed since
January 20, 2016
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 (3)

Package NDCDescriptionSince
68462-357-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-01)Jan 20, 2016
68462-357-05500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-05)Jan 20, 2016
68462-357-9090 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-90)Jun 1, 2016

Recalls mentioning this NDC

Other Potassium Chloride products