Class II · Moderate risk
Rifampin for Injection
Failed Impurities/Degradation Specifications: High out of specification results obtained for related compound during stability testing.
National Drug Code
Is NDC 67457-0445-60 recalled?
Rifampin · 1 VIAL in 1 CARTON (67457-445-60) / 10 mL in 1 VIAL
Yes — this exact package was recalled
2 FDA recalls name the code 67457-0445-60 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
- Rifampin
- Strength
- RIFAMPIN 600 mg/10mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Mylan Institutional LLC
- Type
- Human Prescription Drug
- Product code
- 67457-0445
Recalls naming this package
Class II · Moderate risk
Rifampin for Injection
Failed Impurities/Degradation Specifications: discoloration due to elevated unknown impurity results which could decrease the effectiveness of the product.
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
- 67457-0187 Aloprim 1
- 67457-0196 Thiamine Hydrochloride 1
- 67457-0197 Tranexamic Acid 1
- 67457-0218 Duraclon 1
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.