Class III · Low risk
Folic Acid Injection
Failed Impurities/Degradation specifications: out-of-specification results 14 & 15 month time point
National Drug Code
Is NDC 63323-0184-11 recalled?
Folic Acid
Yes — this exact package was recalled
2 FDA recalls name the code 63323-0184-11 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Folic Acid
- Strength
- FOLIC ACID 5 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous, Subcutaneous
- Labeler
- Fresenius Kabi USA, LLC
- Type
- Human Prescription Drug
- Product code
- 63323-0184
Recalls naming this package
Class III · Low risk
Folic Acid Injection
Failed Impurities/Degradation Specification
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
- 63323-0162 Ketorolac Tromethamine 4
- 63323-0010 Gentamicin 2
- 63323-0186 Sodium Chloride 2
- 63323-0269 Diprivan 2
- 63323-0365 See recall 2
- 63323-0403 Fosphenytoin 2
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.