NDC 66116-352
Citalopram Hydrobromide 20 mg tablet, film coated
On the label: MedVantx, Inc.. It's repackaged from NDC 55111-343, 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). 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 MedVantx, Inc. names for other drugs.
Product details
- Generic drug
- Citalopram: every company that makes it
- Form
- tablet, film coated
- Strength
- 20 mg
- Approval
- ANDA ANDA077038
- On the market since
- Oct 28, 2004
- Package NDCs
66116-352-30- Official label
- DailyMed (National Library of Medicine), updated Jan 7, 2013
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