NDC 0517-4002
Papaverine Hydrochloride 30 mg per 1 mL injection, solution
On the label: American Regent, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | Shirley, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyApr 24, 2024 · 12 inspections, 1 with FDA action |
Recalls
- Jul 24, 2026 · Class I · American Regent, Inc.
Presence of Particulate Matter: Product contaminated with particulate matter identified as glass and/or paraformaldehyde
Lots: Lot #: 25202, Exp. Date: 11/30/2026.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Papaverine: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 30 mg per 1 mL
- Approval
- unapproved drug other
- On the market since
- Sep 1, 1995
- Package NDCs
0517-4002-010517-4002-25- Official label
- DailyMed (National Library of Medicine), updated Jul 27, 2026
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