Class III · Low risk
Mycophenolate Mofetil for Oral Suspension
Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
National Drug Code
Is NDC 66689-0307-08 recalled?
Mycophenolate Mofetil · 1 BOTTLE, PLASTIC in 1 CARTON (66689-307-08) / 250 mL in 1 BOTTLE, PLASTIC
Yes — this exact package was recalled
1 FDA recall names the code 66689-0307-08 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
- Mycophenolate Mofetil
- Strength
- MYCOPHENOLATE MOFETIL 200 mg/mL
- Form
- Powder, for Suspension · Oral
- Labeler
- VistaPharm, LLC
- Type
- Human Prescription Drug
- Product code
- 66689-0307
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
- 66689-0037 See recall 5
- 66689-0008 See recall 4
- 66689-0023 See recall 3
- 66689-0031 See recall 3
- 66689-0036 See recall 3
- 66689-0038 See recall 3
Free recall alerts
Know the day your medication is recalled
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