NDC 33342-417 – Potassium chloride

Potassium Chloride 600 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC33342-417

Product details

Brand name
Potassium chloride
Generic name
Potassium chloride
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA212987
Marketed since
September 8, 2024
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 (4)

Package NDCDescriptionSince
33342-417-11100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-417-11)Sep 8, 2024
33342-417-1210 BLISTER PACK in 1 CARTON (33342-417-12) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKSep 8, 2024
33342-417-15500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-417-15)Sep 8, 2024
33342-417-3410 BLISTER PACK in 1 CARTON (33342-417-34) / 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKSep 8, 2024

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