Ringers

NDC 0990-7982 · ICU Medical, Inc.

Generic nameSODIUM CHLORIDE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM CHLORIDE

Strength33; 30; 860 mg/100mL; mg/100mL; mg/100mL

Pharmacologic classBlood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC]

Marketing categoryNDA

Packages

0990-7982-09 — 12 POUCH in 1 CASE (0990-7982-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0990-7924 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 0990-7925 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 0990-7926 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 0990-7929 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE, 0990-7941 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 0990-7953 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, and CALCIUM CHLORIDE, 0990-7965 — dextrose monohydrate, sodium chloride, potassium acetate, and magnesium acetate, 0990-7967 — SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE, 0990-7968 — Dextrose, Sodium Chloride, Sodium Acetate Anhydrous, Sodium Gluconate, Potassium Chloride, and Magnesium Chloride, 0990-7972 — SODIUM CHLORIDE, 0990-7983 — SODIUM CHLORIDE, 0990-7984 — SODIUM CHLORIDE, 0990-7985 — SODIUM CHLORIDE, 0990-7993 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 0990-9257 — SODIUM CHLORIDE and POTASSIUM CHLORIDE, 10135-807 — Potassium Chloride for Oral Solution, 10135-819 — Potassium Chloride for Oral Solution, 10135-820 — Potassium Chloride for Oral Solution, 10572-100 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 10572-302 — polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloride, +1490 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.