NDC 53002-4850
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: RPK Pharmaceuticals, Inc.. It's repackaged from NDC 0591-3041, made by Actavis Pharma, 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 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 RPK Pharmaceuticals, Inc. names for other drugs.
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated
- Strength
- 200 mg
- Approval
- ANDA ANDA040133
- On the market since
- Mar 30, 2016
- Package NDCs
53002-4850-253002-4850-6- Official label
- DailyMed (National Library of Medicine), updated Dec 16, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?