NDC 14537-966

AS 3

Dextrose Monohydrate, Sodium Citrate, Sodium Chloride, Sodium Phosphate, Monobasic, Monohydrate, Citric Acid Monohydrate And Adenine

AS 3 is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Terumo Bct Ltd. The primary component is Dextrose Monohydrate; Sodium Citrate, Unspecified Form; Sodium Chloride; Sodium Phosphate, Monobasic, Monohydrate; Citric Acid Monohydrate; Adenine.

• Product ID: 14537-966_1f7b74b9-e7df-41fc-9af6-cf7c340300f5
• NDC: 14537-966
• Product Type: Human Prescription Drug
• Proprietary Name: AS 3
• Generic Name: Dextrose Monohydrate, Sodium Citrate, Sodium Chloride, Sodium Phosphate, Monobasic, Monohydrate, Citric Acid Monohydrate And Adenine
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2002-05-29
• Marketing Category: NDA / NDA
• Application Number: BN001214
• Labeler Name: Terumo BCT Ltd
• Substance Name: DEXTROSE MONOHYDRATE; SODIUM CITRATE, UNSPECIFIED FORM; SODIUM CHLORIDE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; CITRIC ACID MONOHYDRATE; ADENINE
• Active Ingredient Strength: 1 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
• 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 14537-966-10

6 POUCH in 1 CASE (14537-966-10) > 6 BAG in 1 POUCH > 100 mL in 1 BAG

• Marketing Start Date: 2002-05-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 14537-966-10 [14537096610]

AS 3 INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: BN001214
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2002-05-29

NDC 14537-966-20 [14537096620]

AS 3 INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: BN001214
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-09-18

Drug Details

Active Ingredients

Ingredient	Strength
DEXTROSE MONOHYDRATE	1.1 g/100mL

OpenFDA Data

• SPL SET ID: 5f51ab45-2ff0-4b07-9fb9-69789da65d4b
• Manufacturer:
  • Terumo BCT Ltd
• UNII:
  • 1Q73Q2JULR
  • 451W47IQ8X
  • LX22YL083G
  • 593YOG76RN
  • 2968PHW8QP
  • JAC85A2161

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]
• 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]