Prescribing information (package insert) - Acd-a
DESCRIPTION
Re-Order Product Code: 796-08
750 mL volume. Single use container.
Sterile, nonpyrogenic fluid path. Sterilized by steam.
Store at room temperature.
INDICATIONS AND USAGE
For use with automated pheresis equipment only. Use according to equipment manufacturer’s instructions. This unit should be used for pheresis only.
CONTRAINDICATIONS
Not for direct intravenous infusion.
WARNINGS
Avoid excessive heat. Protect from freezing.
PRECAUTIONS
Do not use unless solution is clear and no leaks detected.
General
Rx only. Discard unused portion.
Recommended Storage: Store at room temperature (25°C / 77°F).
HOW SUPPLIED
750 mL volume bag.
Each 100 ml contains:
0.73 g citric acid (anhydrous), USP
2.20 g sodium citrate (dihydrate), USP
2.45 g dextrose (monohydrate), USP
References
HAEMONETICS and THE Blood Management Company are trademarks of Haemonetics Corporation.
Manufactured for:
Haemonetics Corporation
400 Wood Road
Braintree, MA 02184, USA
By: Haemonetics Manufacturing Inc.
1630 Industrial Park Street
Covina, CA 91722, USA
About this document
Source: FDA drug labeling via NLM DailyMed · Application number: NDA 710497
· View the label on DailyMed
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The information on this site does not replace the advice of a doctor or pharmacist.
Drug information for Acd-a
| Rx or OTC |
Prescription (Rx)?
- This drug is available only with a prescription from a licensed healthcare provider.
- Rx
|
| Drug class |
Anti-coagulant, Calculi Dissolution Agent |
| Active ingredients |
Dextrose monohydrate 2.45 g/100 mL,
Sodium citrate 2.2 g/100 mL,
Citric acid monohydrate 0.73 g/100 mL
|
| Dosage form |
Solution |
| Route |
Intravenous |
| Marketing status |
not in the current FDA NDC Directory |
| Company (applicant) |
Haemonetics Manufacturing Inc |
| FDA approval |
NDA 710497New Drug Application (NDA)
|
| Manufacturers |
1 labelers list this drug on DailyMed |
| Packages (NDC) |
| Package |
|
2.45 g/100 mL, 2.20 g/100 mL, 0.73 g/100 mL – 750 ml in 1 bag / 12 in 1 carton
NDC 53157-796-08
|
|
Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.
