NDC 0093-2401
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: Teva Pharmaceuticals USA, Inc..
Where it's made
This label doesn't name the factory that makes the drug. 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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA040081
- On the market since
- Oct 8, 2020
- Package NDCs
0093-2401-01- Official label
- DailyMed (National Library of Medicine), updated Feb 29, 2024
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