NDC 71610-047
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged from NDC 0781-5994, made by Sandoz Inc (Hydroxychloroquine Sulfate). 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 Aphena Pharma Solutions - Tennessee, Inc. names for other drugs.
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated
- Strength
- 200 mg
- Approval
- ANDA ANDA040104
- On the market since
- Nov 30, 1995
- Package NDCs
71610-047-60- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?