NDC 68788-8262 – Potassium Chloride

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

Human Prescription Drug

Product NDC68788-8262

Product details

Brand name
Potassium Chloride
Generic name
Potassium Chloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210921
Marketed since
September 19, 2022
Listing expires
December 31, 2027
Pharmacologic class
Osmotic Laxative; Potassium Salt

Active ingredients

Uses, dosage, side effects and warnings for Potassium Chloride →

Package NDC codes (3)

Package NDCDescriptionSince
68788-8262-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8262-3)Sep 19, 2022
68788-8262-660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8262-6)Sep 19, 2022
68788-8262-990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8262-9)Sep 19, 2022

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