NDC 65862-987 – Potassium Chloride

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

Human Prescription Drug

Product NDC65862-987

Product details

Brand name
Potassium Chloride
Generic name
Potassium Chloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210921
Marketed since
December 19, 2018
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 (4)

Package NDCDescriptionSince
65862-987-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-987-01)Dec 19, 2018
65862-987-12120 BLISTER PACK in 1 CARTON (65862-987-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-987-06)Dec 19, 2018
65862-987-8080 BLISTER PACK in 1 CARTON (65862-987-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-987-04)Dec 19, 2018
65862-987-991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-987-99)Dec 19, 2018

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