NDC 53157-136

Leukotrap WB System

Cpda-1 Blood Bag Collection System

Leukotrap WB System is a Intravenous Solution in the Human Prescription Drug category. It is labeled and distributed by Haemonetics Manufacturing Inc. The primary component is Dextrose Monohydrate; Sodium Citrate; Citric Acid Monohydrate; Sodium Phosphate, Monobasic, Monohydrate; Adenine.

• Product ID: 53157-136_8906bc0f-cb7b-ed22-e053-2a95a90ad822
• NDC: 53157-136
• Product Type: Human Prescription Drug
• Proprietary Name: Leukotrap WB System
• Generic Name: Cpda-1 Blood Bag Collection System
• Dosage Form: Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 1980-11-06
• Marketing Category: NDA / NDA
• Application Number: BN800077
• Labeler Name: Haemonetics Manufacturing Inc
• Substance Name: DEXTROSE MONOHYDRATE; SODIUM CITRATE; CITRIC ACID MONOHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; ADENINE
• Active Ingredient Strength: 2 g/70mL; g/70mL; g/70mL; g/70mL; g/70mL
• Pharm Classes: Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 53157-136-94

18 BAG in 1 CARTON (53157-136-94) > 70 mL in 1 BAG

• Marketing Start Date: 1980-11-06
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 53157-136-94 [53157013694]

Leukotrap WB System SOLUTION

• Marketing Category: NDA
• Application Number: BN800077
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1980-11-06

NDC 53157-136-93 [53157013693]

Leukotrap WB System SOLUTION

• Marketing Category: NDA
• Application Number: BN800077
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1980-11-06

NDC 53157-136-92 [53157013692]

Leukotrap WB System SOLUTION

• Marketing Category: NDA
• Application Number: BN800077
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1980-11-06

Drug Details

Active Ingredients

Ingredient	Strength
DEXTROSE MONOHYDRATE	2.23 g/70mL

OpenFDA Data

• SPL SET ID: fdd00e7b-039a-48a8-b654-941f85f5c00f
• Manufacturer:
  • Haemonetics Manufacturing Inc
• UNII:
  • 593YOG76RN
  • 1Q73Q2JULR
  • 2968PHW8QP
  • JAC85A2161
  • LX22YL083G

Pharmacological Class

• Acidifying Activity [MoA]
• Calculi Dissolution Agent [EPC]
• Anti-coagulant [EPC]
• Decreased Coagulation Factor Activity [PE]
• Calcium Chelating Activity [MoA]
• Acidifying Activity [MoA]
• Calculi Dissolution Agent [EPC]
• Anti-coagulant [EPC]
• Decreased Coagulation Factor Activity [PE]
• Calcium Chelating Activity [MoA]

NDC Crossover Matching brand name "Leukotrap WB System" or generic name "Cpda-1 Blood Bag Collection System"

NDC	Brand Name	Generic Name
53157-136	Leukotrap WB System	CPDA-1 Blood Bag Collection System
53157-262	Leukotrap WB System	Leukotrap WB System
53157-736	Leukotrap WB System	CPDA-1 Blood Bag Collection System