Class II · Moderate risk
Bicillin L-A
CGMP Deviations; particulates identified during visual inspection
National Drug Code
Is NDC 60793-0701-02 recalled?
Bicillin L-A
Yes — this exact package was recalled
1 FDA recall names the code 60793-0701-02 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.
1 of these recalls is still ongoing.
- Active ingredient
- penicillin G benzathine
- Strength
- PENICILLIN G BENZATHINE 1200000 [iU]/2mL
- Form
- Injection, Suspension · Intramuscular
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Type
- Human Prescription Drug
- Product code
- 60793-0701
Recalls naming this package
Class II · Moderate risk
Bicillin L-A
cGMP Deviations: Products were stored outside the drug label specifications.
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
- 60793-0851 Levoxyl 3
- 60793-0855 Levoxyl 3
- 60793-0858 Levoxyl 3
- 60793-0860 Levoxyl 3
- 60793-0850 Levoxyl 2
- 60793-0852 Levoxyl 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.