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United States · US · US:0065-8150_7f324d32-7a86-4976-b0f4-b80283e5fc29

PATADAY ONCE DAILY 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 · 4

  • ndc11
    0065815001
    1 BOTTLE, PLASTIC in 1 CARTON (0065-8150-01) / 2.5 mL in 1 BOTTLE, PLASTIC
  • ndc11
    0065815003
    2 BOTTLE, PLASTIC in 1 CARTON (0065-8150-03) / 2.5 mL in 1 BOTTLE, PLASTIC
  • ndc11
    0065815004
    1 BOTTLE, PLASTIC in 1 CARTON (0065-8150-04) / .5 mL in 1 BOTTLE, PLASTIC
  • ndc11
    0065815007
    3 BOTTLE, PLASTIC in 1 CARTON (0065-8150-07) / 2.5 mL in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
2XG66W44KF
OLOPATADINE HYDROCHLORIDE
RxCUI 236599
Orange Book
N021545
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": "0065-8150_7f324d32-7a86-4976-b0f4-b80283e5fc29",
  "productndc": "0065-8150",
  "dosage_form": "SOLUTION",
  "orange_book": {
    "appl_no": "021545",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "EQ 0.2% BASE",
        "product_no": "001",
        "approval_date": "Dec 22, 2004"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OLOPATADINE HYDROCHLORIDE",
  "proprietary_name": "PATADAY ONCE DAILY RELIEF",
  "active_ingred_unit": "mg/mL",
  "application_number": "NDA021545",
  "marketing_category": "NDA",
  "nonproprietary_name": "OLOPATADINE HYDROCHLORIDE",
  "start_marketing_date": "20200228",
  "active_numerator_strength": "2"
}

Related drugs

Other records sharing ATC code R01AC08.

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