- Product NDC
- 14537-966
- 11-digit product format
- 145370966
- Labeler code
- 14537
- Product ID
- 14537-966_1f7b74b9-e7df-41fc-9af6-cf7c340300f5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dextrose Monohydrate, Sodium Citrate, Sodium Chloride, Sodium Phosphate, Monobasic, Monohydrate, Citric Acid Monohydrate and Adenine
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Terumo BCT Ltd
- Application
- BN001214
- Marketing category
- NDA
- Marketing start
- 2002-05-29
- Marketing end
- 0000-00-00
- Substance
- DEXTROSE MONOHYDRATE; SODIUM CITRATE, UNSPECIFIED FORM; SODIUM CHLORIDE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; CITRIC ACID MONOHYDRATE; ADENINE
- Active strength
- 1 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
- Pharmacologic 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
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record