NDC 24208-735
Cyclopentolate Hydrochloride 10 mg per 1 mL solution/ drops
On the label: Bausch & Lomb Incorporated.
Where it's 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 |
Recalls
- Jan 18, 2016 · Class III · Bausch & Lomb, Inc.
Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.
Lots: a) Lot #: 199691, Expiry: 02/2016; Lot # 221481, Expiry: 03/2016, Lot #: 223921, Expiry: 05/2016; Lot #: 226211, Expiry: 06/2016; Lot #: 228611, Expiry: 08/2016; Lot #: 230711, Expiry: 09/2016; Lot #: 232591, Expiry: 11/2016; Lot #: 234551, Expiry: 12/2016; Lot #: 238871, Expiry: 01/2017; Lot #: 23…
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Cyclopentolate: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA040075
- On the market since
- Apr 29, 1994
- Package NDCs
24208-735-0124208-735-06- Official label
- DailyMed (National Library of Medicine), updated Sep 29, 2022
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