Class III ยท Low risk
Ampicillin for Injection
Labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
National Drug Code
Is NDC 0781-3407-95 recalled?
Ampicillin · 10 VIAL, GLASS in 1 PACKAGE (0781-3407-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-3407-78)
Yes — this exact package was recalled
1 FDA recall names the code 0781-3407-95 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
- Ampicillin sodium
- Strength
- AMPICILLIN SODIUM 500 mg/1
- Form
- Injection, Powder, for Solution · Intramuscular, Intravenous
- Labeler
- Sandoz Inc
- Type
- Human Prescription Drug
- Product code
- 0781-3407
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
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.