NDC 43598-678
Azacitidine Azacitidine 100 mg injection, powder, lyophilized, for solution
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Shilpa Medicare Limited | Mahabubnagar, India | Makes it and tests it | Serious problems, FDA actionFeb 25, 2020 · 6 inspections, 1 with FDA action |
Product details
- Generic drug
- Azacitidine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous; subcutaneous
- Strength
- 100 mg
- Approval
- ANDA ANDA207518
- On the market since
- Dec 13, 2017
- Package NDCs
43598-678-11- Official label
- DailyMed (National Library of Medicine), updated Jul 20, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?