Class III ยท Low risk
Lotemax (loteprednol etabonate ophthalmic gel 0.5%)
Failed Stability Specifications: Out of specification for viscosity.
National Drug Code
Is NDC 24208-0503-07 recalled?
Lotemax · 1 BOTTLE in 1 CARTON (24208-503-07) / 5 g in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 24208-0503-07 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- loteprednol etabonate
- Strength
- LOTEPREDNOL ETABONATE 5 mg/g
- Form
- Gel · Ophthalmic
- Labeler
- Bausch & Lomb Incorporated
- Type
- Human Prescription Drug
- Product code
- 24208-0503
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 24208-0280 See recall 1
- 24208-0385 Muro 128 1
- 24208-0439 See recall 1
- 24208-0507 Lotemax SM 1
- 24208-0539 Miochol E 1
- 24208-0585 Tropicamide 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.