NDC 68071-3880
Ketorolac Tromethamine 5 mg per 1 mL solution/ drops
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Apotex Corp.'s NDC 60505-1003.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Apotex Corp. names for other drugs.
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Recalls
- Sep 5, 2025 · Class II · Apotex Corp.
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
Lots: Batch # VA0444, exp. date 01/2026 Batch # VA4608, exp. date 01/2026 Batch # TZ7016, exp. date 12/2025 UPC on Bottles: (01)0(03)60505100316 UPC on Cartons: 360505100316 - May 28, 2025 · Class II · Apotex Corp.
Lack of Assurance of Sterility
Lots: Batch TZ1236, Exp Date: 11/30/2025
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
- solution/ drops, ophthalmic
- Strength
- 5 mg per 1 mL
- Approval
- ANDA ANDA076109
- On the market since
- Dec 7, 2009
- Package NDCs
68071-3880-5- Official label
- DailyMed (National Library of Medicine), updated Jul 31, 2025
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