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United States · US · US:24208-601_4f27a942-b5f3-4a01-8022-49deced585f8
Alaway
Orange BookUNIIATC R06AX17
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBausch & Lomb Incorporated
CountryUS (United States)
ATC codeR06AX17
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1124208601051 BOTTLE, DROPPER in 1 CARTON (24208-601-05) / 5 mL in 1 BOTTLE, DROPPER
- ndc1124208601101 BOTTLE, DROPPER in 1 CARTON (24208-601-10) / 10 mL in 1 BOTTLE, DROPPER
- ndc1124208601902 BOTTLE, DROPPER in 1 CARTON (24208-601-90) / 10 mL in 1 BOTTLE, DROPPER
Annotations
UNII (FDA Substance ID)
HBD503WORO
KETOTIFEN FUMARATE
RxCUI 11404
Orange Book
N021996
Raw payload (JSON)
{
"unii": {
"unii": "HBD503WORO",
"rxcui": "11404",
"inchikey": "YNQQEYBLVYAWNX-WLHGVMLRSA-N",
"display_name": "KETOTIFEN FUMARATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "OPHTHALMIC",
"productid": "24208-601_4f27a942-b5f3-4a01-8022-49deced585f8",
"productndc": "24208-601",
"dosage_form": "SOLUTION/ DROPS",
"orange_book": {
"appl_no": "021996",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "EQ 0.025% BASE",
"product_no": "001",
"approval_date": "Dec 1, 2006"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "EQ 0.025% BASE",
"product_no": "002",
"approval_date": "Feb 11, 2015"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "KETOTIFEN FUMARATE",
"proprietary_name": "Alaway",
"active_ingred_unit": "mg/mL",
"application_number": "NDA021996",
"marketing_category": "NDA",
"nonproprietary_name": "Ketotifen Fumarate",
"start_marketing_date": "20061201",
"active_numerator_strength": ".25"
}Related drugs
Other records sharing ATC code R06AX17.
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