Class II · Moderate risk
C-*Vancomycin Opthal 14 mg drops
Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.
National Drug Code
Is NDC 67457-0340-01 recalled?
Vancomycin Hydrochloride · 10 VIAL in 1 CARTON (67457-340-01) / 20 mL in 1 VIAL (67457-340-00)
Yes — this exact package was recalled
1 FDA recall names the code 67457-0340-01 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
- Vancomycin Hydrochloride
- Strength
- VANCOMYCIN HYDROCHLORIDE 1 g/20mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Mylan Institutional LLC
- Type
- Human Prescription Drug
- Product code
- 67457-0340
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
- 67457-0153 Amiodarone Hydrochloride 2
- 67457-0386 Mycophenolate Mofetil 2
- 67457-0445 Rifampin 2
- 67457-0187 Aloprim 1
- 67457-0196 Thiamine Hydrochloride 1
- 67457-0197 Tranexamic Acid 1
Free recall alerts
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