NDC 43598-389
Docetaxel 160 mg per 8 mL injection, solution
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr.reddy's Laboratories Limited | Visakhapatnam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 17, 2024 · 9 inspections, 2 with FDA action |
Recalls
- Mar 6, 2019 · Class II · Dr. Reddy's Laboratories, Inc.
Defective Container: complaint for seal and cap vial issues that could lead to a lack of sterility assurance.
Lots: Lot#: H7081, Exp 07/2019
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Docetaxel: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 160 mg per 8 mL
- Approval
- ANDA ANDA204193
- On the market since
- Apr 22, 2019
- Package NDCs
43598-389-57- Official label
- DailyMed (National Library of Medicine), updated Jun 23, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?