NDC 23155-294
Prochlorperazine Edisylate 5 mg per 1 mL injection
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Emcure Pharmaceuticals Limited | Ahmedabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 15, 2026 · 3 inspections |
Recalls
- May 21, 2019 · Class I · Heritage Pharmaceuticals, Inc.
Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate Injection, USP 1gm/4 mL (250mg/mL) and Prochlorperazine Edisylate Injection, USP 10mg/2mL (5mg/mL) .
Lots: Lot: VPCA172, EXP April 2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Prochlorperazine: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 5 mg per 1 mL
- Approval
- ANDA ANDA204147
- On the market since
- Mar 26, 2012
- Package NDCs
23155-294-3123155-294-4123155-294-42- Official label
- DailyMed (National Library of Medicine), updated Mar 11, 2025
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