NDC 67296-1780
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: RedPharm Drug. 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 RedPharm Drug. 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
- Jan 1, 2020
- Package NDCs
67296-1780-1- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?