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ACD Blood-Pack Units (PL 146 PLASTIC)

NDC 0942-9001 · Fenwal, Inc.

Generic nameAnticoagulant Citrate Dextrose (ACD)
Dosage formSOLUTION
RouteINTRAVENOUS
Active ingredient(s)DEXTROSE MONOHYDRATE, TRISODIUM CITRATE DIHYDRATE, ANHYDROUS CITRIC ACID
Strength493; 1.65; 1.48 mg/67.5mL; g/67.5mL; g/67.5mL
Pharmacologic classAcidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE]
Marketing categoryNDA

Packages

0942-9001-01 — 67.5 mL in 1 BAG (0942-9001-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0941-0735 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, 0942-0641 — Anticoagulant Citrate Dextrose Solution Formula A, 0942-6305 — Anticoagulant Citrate Phosphate Dextrose Adenine, 0942-6307 — Anticoagulant Citrate Phosphate Dextrose Adenine, 0942-6308 — Anticoagulant Citrate Phosphate Dextrose Adenine, 0942-6312 — Anticoagulant Citrate Phosphate Dextrose Adenine, 0942-6316 — Anticoagulant Citrate Phosphate Dextrose Adenine, 0942-6320 — Anticoagulant Citrate Phosphate Dextrose Adenine, 0942-6322 — Anticoagulant Citrate Phosphate Dextrose Adenine, 0942-6326 — Anticoagulant Citrate Phosphate Dextrose Adenine, 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, 0942-9601 — Platelet Additive 3, 0942-9602 — Platelet Additive 3, +264 more

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