NDC 52652-8001
Zonisade 100 mg per 5 mL suspension
On the label: Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals).
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 Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) names for other drugs.
Product details
- Generic drug
- Zonisamide: every company that makes it
- Form
- suspension, oral
- Strength
- 100 mg per 5 mL
- Approval
- NDA NDA214273
- On the market since
- Jul 15, 2022
- Package NDCs
52652-8001-1- Official label
- DailyMed (National Library of Medicine), updated Sep 8, 2025
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