NDC 68645-282
Citalopram hydrobromide 40 mg tablet
On the label: Legacy Pharmaceutical Packaging. It's repackaged from NDC 55111-344, made by Dr. Reddy's Laboratories Limited (Citalopram Hydrobromide). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Legacy Pharmaceutical Packaging names for other drugs.
Product details
- Generic drug
- Citalopram: every company that makes it
- Form
- tablet
- Strength
- 40 mg
- Approval
- ANDA ANDA077038
- On the market since
- Oct 1, 2010
- Package NDCs
68645-282-54- Official label
- DailyMed (National Library of Medicine), updated Feb 23, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?