Where it's 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 Leadiant Biosciences, Inc. names for other drugs.
Recalls
- Sep 24, 2020 · Class III · Leadiant Biosciences, Inc.
Subpotent Drug: Product testing identified a decreased level of the active ingredient, Cysteamine HCl.
Lots: Lot #: 370655, Exp. 10/31/2020 - Apr 9, 2018 · Class III · Leadiant Biosciences, Inc
Subpotent drug: Out of specification for an active ingredient cysteamine hydrochloride.
Lots: lot numbers: 35866, Exp 6/18; 358663, Exp 7/18 - Feb 14, 2018 · Class III · Leadiant Biosciences, Inc
Subpotent Drug: Out of specification for an active ingredient cysteamine hydrochloride.
Lots: Lot #: 356075, Exp 2/28/18
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Cysteamine: every company that makes it
- Form
- solution, ophthalmic
- Strength
- 6.5 mg per 1 mL
- Approval
- NDA NDA200740
- On the market since
- Dec 30, 2012
- Package NDCs
54482-020-0154482-020-02- Official label
- DailyMed (National Library of Medicine), updated Oct 21, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?