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United States · US · US:24208-353_138577af-1a4e-48fb-b088-47f54c896442
Alrex
Orange BookUNIIATC S01BA14
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBausch & Lomb Incorporated
CountryUS (United States)
ATC codeS01BA14
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1124208353011 BOTTLE, DROPPER in 1 CARTON (24208-353-01) / 1 mL in 1 BOTTLE, DROPPER
- ndc1124208353051 BOTTLE, DROPPER in 1 CARTON (24208-353-05) / 5 mL in 1 BOTTLE, DROPPER
- ndc1124208353101 BOTTLE, DROPPER in 1 CARTON (24208-353-10) / 10 mL in 1 BOTTLE, DROPPER
Annotations
UNII (FDA Substance ID)
YEH1EZ96K6
LOTEPREDNOL ETABONATE
RxCUI 52177
Orange Book
N020803
AB
Raw payload (JSON)
{
"unii": {
"unii": "YEH1EZ96K6",
"rxcui": "52177",
"inchikey": "DMKSVUSAATWOCU-HROMYWEYSA-N",
"display_name": "LOTEPREDNOL ETABONATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "OPHTHALMIC",
"productid": "24208-353_138577af-1a4e-48fb-b088-47f54c896442",
"productndc": "24208-353",
"dosage_form": "SUSPENSION/ DROPS",
"orange_book": {
"appl_no": "020803",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "0.2%",
"product_no": "001",
"approval_date": "Mar 9, 1998"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LOTEPREDNOL ETABONATE",
"proprietary_name": "Alrex",
"active_ingred_unit": "mg/mL",
"application_number": "NDA020803",
"marketing_category": "NDA",
"nonproprietary_name": "loteprednol etabonate",
"start_marketing_date": "19980309",
"active_numerator_strength": "2"
}Related drugs
Other records sharing ATC code S01BA14.
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