Medicine
Lotemax 5 mg/mL ophthalmic suspension
Lotemax 5 mg/mL ophthalmic suspension is a prescription medicine containing Loteprednol etabonate for ophthalmic use, marketed by Bausch & Lomb, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.
Availability
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Ambient
DO NOT FREEZE Keep out of reach of children. Store upright between 15°C to…
Key facts
- Active ingredient (INN)
- Loteprednol etabonate
- Brand
- Lotemax
- Strength
- 5 mg/mL
- Dosage form
- Ophthalmic suspension
- Route
- Ophthalmic
- Packs
- 1 bottle
- Marketing authorisation holder
- Bausch & Lomb
- Manufacturer
- Bausch & Lomb
- Origin register
- US FDA, United States
- Storage
- DO NOT FREEZE Keep out of reach of children. Store upright between 15°C to 25°C (59°F to 77°F).
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- S01BA14 Loteprednol etabonate
- HS code (indicative)
- 3004.32Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 9 March 1998
- Identifiers
- RxCUI 213263, 311382DailyMed set ID f37d74ac-5f9c-40a8-b43b-35148fc66bbeNDC 24208-299Application NDA020583
Record updated 12 November 2026
Documents available
Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.
No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.
Packs
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 1 bottle in 1 carton / 5 mL in 1 bottle | 24208-299-05 | Bausch & Lomb | 3 September 1998 |
| 1 bottle in 1 carton / 10 mL in 1 bottle | 24208-299-10 | Bausch & Lomb | 3 September 1998 |
| 1 bottle in 1 carton / 15 mL in 1 bottle | 24208-299-15 | Bausch & Lomb | 3 September 1998 |
Status by register
Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| US FDA | First approved 9 March 1998 | Drugs@FDA |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US FDA (NDC directory, openFDA)Checked 12 November 2026 |
Import route
Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.
Import guides are available for 25 countries. Pick one to see its route summary.
BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides
Alternatives
Other makers and brands of Loteprednol etabonate 5 mg/mL ophthalmic suspension.
Other strengths and forms of Loteprednol etabonate
Clinical summary
Loteprednol etabonate is a corticosteroid indicated for the treatment of steroid-responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe such as allergic conjunctivitis, among other approved uses. MedsAcross supplies Loteprednol etabonate for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.
Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review
Read about Loteprednol etabonateFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Loteprednol Etabonate prescribing information (Bausch & Lomb Americas) · U.S. National Library of Medicine, DailyMed
Need Lotemax 5 mg/mL ophthalmic suspension for your hospital or patient?
Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.