NDC 59651-276
Propafenone Hydrochloride 225 mg capsule, extended release
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Propafenone: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 225 mg
- Approval
- ANDA ANDA213096
- On the market since
- Feb 21, 2023
- Package NDCs
59651-276-0559651-276-6059651-276-90- Official label
- DailyMed (National Library of Medicine), updated Feb 4, 2025
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