Class I ยท High risk
Buffered Penicillin G Potassium for Injection
Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for Injection, USP, 20 million Unit
National Drug Code
Is NDC 0781-6136-94 recalled?
Penicillin G Potassium · 1 VIAL in 1 CARTON (0781-6136-94) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 0781-6136-94 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.
1 of these recalls is still ongoing.
- Active ingredient
- Penicillin G Potassium
- Strength
- PENICILLIN G POTASSIUM 20000000 [iU]/1
- Form
- Injection, Powder, for Solution · Intramuscular, Intravenous
- Labeler
- Sandoz Inc
- Type
- Human Prescription Drug
- Product code
- 0781-6136
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.