Class II ยท Moderate risk
Docetaxel Injection USP
Defective Container: complaint for seal and cap vial issues that could lead to a lack of sterility assurance.
National Drug Code
Is NDC 43598-0259-40 recalled?
Docetaxel · 4 mL in 1 VIAL, GLASS (43598-259-40)
Yes — this exact package was recalled
1 FDA recall names the code 43598-0259-40 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
- Docetaxel
- Strength
- DOCETAXEL 80 mg/4mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Dr. Reddy's Laboratories Inc.
- Type
- Human Prescription Drug
- Product code
- 43598-0259
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
- 43598-0315 Amlodipine besylate and Atorvastatin calcium 2
- 43598-0405 Phytonadione Phytonadione 2
- 43598-0477 See recall 2
- 43598-0510 Esomeprazole Magnesium 2
- 43598-0561 Lansoprazole 2
- 43598-0743 Ezetimibe and Simvastatin 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.