NDC 31722-307
Ketorolac Tromethamine 60 mg per 2 mL injection, solution
On the label: Camber Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aspiro Pharma Limited | Siddipet, India | Makes it | Problems found, fixed voluntarilyAug 11, 2023 · 1 inspection |
Recalls
- Oct 1, 2025 · Class II · Aspiro Pharma Limited
Presence of Particulate Matter: Particulate matter identified as glass
Lots: Lot #: AS1240347A, Exp Date 09/2026; AS1240144A, Exp Date 05/2026; AS1240145A, AS1240146A, Exp Date 06/2026; AS1250295A, Exp Date 05/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ketorolac: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 60 mg per 2 mL
- Approval
- ANDA ANDA217166
- On the market since
- Jun 20, 2023
- Package NDCs
31722-307-25- Official label
- DailyMed (National Library of Medicine), updated Oct 4, 2024
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