NDC 68071-4368
Proparacaine Hydrochloride 5 mg per 1 mL solution/ drops
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Bausch & Lomb Incorporated's NDC 24208-730.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bausch & Lomb Incorporated | Tampa, FL, United States | Makes it | Serious problems, FDA actionMar 20, 2026 · 17 inspections, 3 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Recalls
- Sep 11, 2024 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
Temperature abuse: Products exposed to improper temperature above drug label specifications.
Lots: Lot # 476261, 479751, 479741, Exp 3/31/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Proparacaine: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 5 mg per 1 mL
- Approval
- ANDA ANDA040074
- On the market since
- Sep 29, 1995
- Package NDCs
68071-4368-5- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2024
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