NDC 59651-773
prochlorperazine maleate 5 mg tablet, film coated
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
- Prochlorperazine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA218734
- On the market since
- Sep 8, 2025
- Package NDCs
59651-773-01- Official label
- DailyMed (National Library of Medicine), updated Sep 11, 2025
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