Loteprednol Etabonate
NDC 24208-508, loteprednol etabonate, gel, from Bausch & Lomb Incorporated.
- Product NDC
- 24208-508
- Status
- Listed
- Labeler
- Bausch & Lomb Incorporated
- Dosage form
- GEL
- Route
- OPHTHALMIC
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA202872
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/24208-508 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LOTEPREDNOL ETABONATE5 mg/g
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 24208-508-01 | 24208050801 | 1 BOTTLE in 1 CARTON (24208-508-01) / 5 g in 1 BOTTLE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/7bbdbd31-5a8f-4d69-aa8e-5b700895e804NADAC price for package 24208050801
GET /v1/drugs/nadac/24208050801
Use it
Look up 24208-508 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/24208-508 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 24208-508. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.