Class II · Moderate risk
PHENOBARBITAL Sodium Injection
Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
National Drug Code
Is NDC 42494-0416-03 recalled?
Phenobarbital Sodium · 3 VIAL in 1 BOX, UNIT-DOSE (42494-416-03) / 1 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 42494-0416-03 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
- Phenobarbital Sodium
- Strength
- PHENOBARBITAL SODIUM 130 mg/mL
- Form
- Injection · Intramuscular
- Labeler
- Cameron Pharmaceuticals
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 42494-0416
Recalls naming this package
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
- 42494-0415 Phenobarbital Sodium 1
- 42494-0437 See recall 1
- 42494-0448 See recall 1
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