NDC 0480-2602
Dextromethorphan hydrobromide and quinidine sulfate 10 mg / 20 mg capsule
On the label: Teva Pharmaceuticals, 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, Inc. names for other drugs.
Product details
- Generic drug
- Dextromethorphan and Quinidine: every company that makes it
- Form
- capsule, oral
- Strength
- 10 mg / 20 mg
- Approval
- ANDA ANDA202934
- On the market since
- Sep 16, 2026
- Package NDCs
0480-2602-06- Official label
- DailyMed (National Library of Medicine), updated Apr 1, 2026
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