NDC 65862-074
Citalopram Hydrobromide 10 mg per 5 mL solution
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Citalopram: every company that makes it
- Form
- solution, oral
- Strength
- 10 mg per 5 mL
- Approval
- ANDA ANDA077812
- On the market since
- Aug 28, 2006
- Package NDCs
65862-074-24- Official label
- DailyMed (National Library of Medicine), updated May 8, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?