NDC 16571-736
Propafenone Hydrochloride 225 mg capsule, extended release
On the label: Rising Pharma Holdings, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| USV Private Limited | Daman, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionApr 17, 2026 · 8 inspections, 3 with FDA action |
Product details
- Generic drug
- Propafenone: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 225 mg
- Approval
- ANDA ANDA205956
- On the market since
- Dec 16, 2020
- Package NDCs
16571-736-0616571-736-50- Official label
- DailyMed (National Library of Medicine), updated Sep 30, 2020
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