Class I · High risk
Ketorolac Tromethamine Injection
Presence of Particulate Matter - found in reserve sample vials at the firm.
National Drug Code
Is NDC 63323-0162-02 recalled?
Ketorolac Tromethamine · 25 VIAL, SINGLE-USE in 1 TRAY (63323-162-02) / 2 mL in 1 VIAL, SINGLE-USE (63323-162-03)
Yes — this exact package was recalled
2 FDA recalls name the code 63323-0162-02 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
- Ketorolac Tromethamine
- Strength
- KETOROLAC TROMETHAMINE 30 mg/mL
- Form
- Injection, Solution · Intramuscular
- Labeler
- Fresenius Kabi USA, LLC
- Type
- Human Prescription Drug
- Product code
- 63323-0162
Recalls naming this package
Class II · Moderate risk
Ketorolac Tromethamine Injection
Presence of Particulate Matter - found in reserve sample vials at the firm.
Class II · Moderate risk
Ketorolac Tromethamine Injection
Presence of Particulate Matter - found in reserve sample vials at the firm.
Class I · High risk
Ketorolac Tromethamine Injection
Presence of Particulate Matter - found in reserve sample vials at the firm.
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
- 63323-0010 Gentamicin 2
- 63323-0184 Folic Acid 2
- 63323-0186 Sodium Chloride 2
- 63323-0269 Diprivan 2
- 63323-0365 See recall 2
- 63323-0403 Fosphenytoin 2
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