NDC 71930-026
Brompheniramine maleate, pseudoephedrine hydrochloride, 2 mg per 5 mL / 10 mg per 5 mL / 30 mg per 5 mL syrup
On the label: Eywa Pharma Inc.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Wes Pharma Inc | Westminster, MD, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyNov 20, 2025 · 7 inspections |
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 13120103A
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Brompheniramine and Dextromethorphan and Pseudoephedrine: every company that makes it
- Form
- syrup, oral
- Strength
- 2 mg per 5 mL / 10 mg per 5 mL / 30 mg per 5 mL
- Approval
- ANDA ANDA211170
- On the market since
- Jun 26, 2020
- Package NDCs
71930-026-1871930-026-43- Official label
- DailyMed (National Library of Medicine), updated May 5, 2026
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