SUTAB

NDC 52268-201 · Braintree Laboratories, Inc.

Generic namesodium sulfate, magnesium sulfate, and potassium chloride

Dosage formTABLET

RouteORAL

Active ingredient(s)SODIUM SULFATE, MAGNESIUM SULFATE ANHYDROUS, POTASSIUM CHLORIDE

Strength2.7; 2.25; 17.75 g/1; g/1; g/1

Pharmacologic classCalculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Marketing categoryNDA

Packages

52268-201-01 — 2 BOTTLE, PLASTIC in 1 KIT (52268-201-01) / 12 TABLET in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51655-463 — Potassium Chloride, 51655-568 — potassium chloride, 51655-706 — Potassium Chloride, 51662-1387 — POTASSIUM CHLORIDE, 51662-1421 — POTASSIUM CHLORIDE, 51662-1516 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, 51662-1521 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE, 52268-012 — sodium sulfate, potassium sulfate, magnesium sulfate, 52268-100 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 52268-112 — sodium sulfate, potassium sulfate, magnesium sulfate, 52536-175 — sodium sulfate, potassium sulfate, magnesium sulfate, 52536-177 — sodium sulfate, potassium sulfate, magnesium sulfate, 52536-236 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 52536-302 — polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloride, 53041-420 — Potassium Chloride, 53041-680 — Potassium Chloride, 53041-681 — Potassium Chloride, 53499-1391 — SANGUINARIA CANADENSIS ROOT, GOLDENSEAL, SILICON DIOXIDE, POTASSIUM CHLORIDE, PULSATILLA VULGARIS, 53499-4194 — PELARGONIUM SIDOIDES ROOT, HYDRASTIS CANADENSIS WHOLE, POTASSIUM CHLORIDE, SANGUINARIA CANADENSIS ROOT, PULSATILLA VULGARIS, SILICON DIOXIDE, 53746-542 — Potassium Chloride, +629 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels