NDC 70436-152 – Potassium Chloride

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

Human Prescription Drug

Product NDC70436-152

Product details

Brand name
Potassium Chloride
Generic name
Potassium Chloride
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA212561
Marketed since
February 1, 2020
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
70436-152-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-152-01)Feb 1, 2020
70436-152-031000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-152-03)Feb 1, 2020

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