Class II · Moderate risk
Carton label: Mycophenolate Mofetil for injection
Failed Dissolution Specifications
National Drug Code
Is NDC 67457-0386-00 recalled?
Mycophenolate Mofetil
Yes — this exact package was recalled
2 FDA recalls name the code 67457-0386-00 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.
2 of these recalls are still ongoing.
- Active ingredient
- Mycophenolate Mofetil
- Strength
- MYCOPHENOLATE MOFETIL 500 mg/20mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Mylan Institutional LLC
- Type
- Human Prescription Drug
- Product code
- 67457-0386
Recalls naming this package
Class II · Moderate risk
Mycophenolate Mofetil for Injection USP
Presence of precipitate
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
- 67457-0445 Rifampin 2
- 67457-0187 Aloprim 1
- 67457-0196 Thiamine Hydrochloride 1
- 67457-0197 Tranexamic Acid 1
- 67457-0218 Duraclon 1
Free recall alerts
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