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POTASSIUM CHLORIDE

NDC 63304-078 · Sun Pharmaceutical Industries, Inc.

Generic namePOTASSIUM CHLORIDE
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)POTASSIUM CHLORIDE
Strength600 mg/1
Pharmacologic classIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
Marketing categoryANDA

Packages

63304-078-01 — 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-078-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60687-884 — POTASSIUM CHLORIDE ORAL, 60760-423 — Potassium Chloride, 62037-560 — Potassium Chloride, 62037-720 — Potassium Chloride, 62106-1054 — Potassium Chloride, 62207-726 — Potassium Chloride Extended-release, 62207-727 — Potassium Chloride Extended-release, 62207-914 — Potassium Chloride, 62207-915 — Potassium Chloride, 63304-076 — Potassium Chloride, 63304-090 — POTASSIUM CHLORIDE, 63304-987 — Potassium Chloride, 63323-164 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, 63323-667 — Potassium Chloride, Dextrose Monohydrate, 63323-669 — Potassium Chloride, Dextrose Monohydrate, 63323-683 — Sodium Chloride and Potassium Chloride, 63323-686 — Sodium Chloride and Potassium Chloride, 63323-688 — Sodium Chloride and Potassium Chloride, 63323-965 — POTASSIUM CHLORIDE, 63323-967 — POTASSIUM CHLORIDE, +445 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.