NDC 70748-332
Prednisolone Acetate 10 mg per 1 mL suspension/ drops
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Pithampur, India | Makes it and packages it | Serious problems, FDA actionJul 17, 2025 · 6 inspections, 4 with FDA action |
Recalls
- Jun 4, 2026 · Class II · Lupin Pharmaceuticals Inc.
Presence of Foreign Substance
Lots: Lots: a) HA00937, HA00939, HA00941, HA00971, H00973, HA00975, Expires: 7/31/2026; HA00987, HA00989, HA00991, HA01010, HA01012, HA01014, HA01016, HA01048, Expires: 8/31/2026; HA01120, HA01137, HA01129, HA01138, HA01133, Expires: 9/30/2026; HA01148, HA01196, HA01198, HA01200, HA01206, HA01208, HA012…
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Prednisolone: every company that makes it
- Form
- suspension/ drops, ophthalmic
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA216935
- On the market since
- Oct 11, 2024
- Package NDCs
70748-332-0270748-332-0370748-332-04- Official label
- DailyMed (National Library of Medicine), updated Oct 13, 2025
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