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InterSol

NDC 0942-9601 · Fenwal, Inc.

Generic namePlatelet Additive 3
Dosage formSOLUTION
RouteINTRAVENOUS
Active ingredient(s)SODIUM CHLORIDE, SODIUM ACETATE, TRISODIUM CITRATE DIHYDRATE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Strength442; 452; 305; 93; 318 mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL
Pharmacologic classAcidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]
Marketing categoryNDA

Packages

0942-9601-12 — 500 mL in 1 BAG (0942-9601-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0942-6326 — Anticoagulant Citrate Phosphate Dextrose Adenine, 0942-9001 — Anticoagulant Citrate Dextrose (ACD), 0942-9201 — Anticoagulant Citrate Phosphate Dextrose (CPD) Solution, 0942-9202 — Anticoagulant Citrate Phosphate Dextrose (CPD), 0942-9393 — Anticoagulant Citrate Phosphate Dextrose Adenine, 0942-9394 — Anticoagulant Citrate Phosphate Dextrose Adenine (CPDA-1) Solution, 0942-9398 — Anticoagulant Citrate Phosphate Dextrose Adenine, 0942-9504 — Anticoagulant Sodium Citrate Solution, 0942-9505 — Anticoagulant Sodium Citrate Solution, 0942-9506 — Anticoagulant Sodium Citrate Solution, 0942-9602 — Platelet Additive 3, 0942-9603 — Solucion aditiva para plaquetas 3, 0942-9605 — Platelet Additive 3, 0990-7107 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 0990-7109 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 0990-7111 — POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM LACTATE, and DEXTROSE MONOHYDRATE, 0990-7115 — SODIUM CHLORIDE and POTASSIUM CHLORIDE, 0990-7116 — SODIUM CHLORIDE and POTASSIUM CHLORIDE, 0990-7372 — DEXTROSE MONOHYDRATE, SODIUM LACTATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, POTASSIUM PHOSPHATE, MONOBASIC, and SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, 0990-7670 — SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE, +1099 more

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