🇺🇸
United States · US · US:0065-4274_c2f804cb-30d1-40d1-b48e-06889a3e0490
PATADAY TWICE A DAY RELIEF
Orange BookUNIISPLATC R01AC08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAlcon Laboratories, Inc.
CountryUS (United States)
ATC codeR01AC08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1100654274011 BOTTLE, PLASTIC in 1 CARTON (0065-4274-01) / 5 mL in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
2XG66W44KF
OLOPATADINE HYDROCHLORIDE
RxCUI 236599
Orange Book
N020688
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2XG66W44KF",
"rxcui": "236599",
"inchikey": "HVRLZEKDTUEKQH-NOILCQHBSA-N",
"display_name": "OLOPATADINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "OPHTHALMIC",
"spl_meta": {
"1c7d2342-ba1c-4244-9814-d92a05725d4e": {
"match": "brand_token",
"title": "PATADAY ONCE DAILY RELIEF (OLOPATADINE HYDROCHLORIDE) SOLUTION [ALCON LABORATORIES, INC.]",
"spl_version": "7",
"published_date": "2026-01-23"
}
},
"productid": "0065-4274_c2f804cb-30d1-40d1-b48e-06889a3e0490",
"productndc": "0065-4274",
"dosage_form": "SOLUTION",
"orange_book": {
"appl_no": "020688",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "EQ 0.1% BASE",
"product_no": "001",
"approval_date": "Dec 18, 1996"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OLOPATADINE HYDROCHLORIDE",
"proprietary_name": "PATADAY TWICE A DAY RELIEF",
"active_ingred_unit": "mg/mL",
"application_number": "NDA020688",
"marketing_category": "NDA",
"nonproprietary_name": "OLOPATADINE HYDROCHLORIDE",
"start_marketing_date": "20200225",
"active_numerator_strength": "1"
}Related drugs
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