NDC 53808-1112
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 63304-296, made by Sun Pharmaceutical Industries, 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 State of Florida DOH Central Pharmacy names for other drugs.
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated
- Strength
- 200 mg
- Approval
- ANDA ANDA040766
- On the market since
- Aug 27, 2017
- Package NDCs
53808-1112-1- Official label
- DailyMed (National Library of Medicine), updated Jan 29, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?