National Drug Code
Is NDC 0338-9669-01 recalled?
Anticoagulant Sodium Citrate · 250 mL in 1 BAG (0338-9669-01)
Recall announced for this product
announced by the firm and posted by FDA; not yet in FDA’s classified recall data
-
Anticoagulant Sodium Citrate Solution USP, 250 mL VIAFLEX Plastic Container
· Baxter International Inc. ·
Reason Potential presence of particulate matter identified as fiberglass in the solution
- Active ingredient
- trisodium citrate dihydrate
- Strength
- TRISODIUM CITRATE DIHYDRATE 40 mg/mL
- Form
- Solution · Extracorporeal
- Labeler
- Baxter Healthcare Corporation
- Type
- Human Prescription Drug
- Product code
- 0338-9669
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.