0065-8150 NDC - PATADAY ONCE DAILY RELIEF (OLOPATADINE HYDROCHLORIDE)

Drug Information

Product NDC: 0065-8150

Proprietary Name: PATADAY ONCE DAILY RELIEF

Non Proprietary Name: OLOPATADINE HYDROCHLORIDE

Active Ingredient(s):
  • 2 mg/mL OLOPATADINE HYDROCHLORIDE


Administration Route(s): OPHTHALMIC

Dosage Form(s): SOLUTION

Pharmacy Class(es):
  • Decreased Histamine Release [PE];
  • Histamine H1 Receptor Antagonists [MoA];
  • Histamine-1 Receptor Antagonist [EPC];
  • Histamine-1 Receptor Inhibitor [EPC];
  • Mast Cell Stabilizer [EPC]

Labeler Information

Labeler Name: Alcon Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021545
Marketing Category: NDA
Start Marketing Date:2/28/2020

Package Information

No. Package Code Package Description Billing Unit
10065-8150-011 BOTTLE, PLASTIC in 1 CARTON (0065-8150-01) / 2.5 mL in 1 BOTTLE, PLASTICML
20065-8150-032 BOTTLE, PLASTIC in 1 CARTON (0065-8150-03) / 2.5 mL in 1 BOTTLE, PLASTICML
30065-8150-041 BOTTLE, PLASTIC in 1 CARTON (0065-8150-04) / .5 mL in 1 BOTTLE, PLASTIC
40065-8150-073 BOTTLE, PLASTIC in 1 CARTON (0065-8150-07) / 2.5 mL in 1 BOTTLE, PLASTIC

NDC Record

Field Name Field Value Definition
PRODUCT NDC0065-8150The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEPATADAY ONCE DAILY RELIEFThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEOLOPATADINE HYDROCHLORIDEThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEOPHTHALMICThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/28/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMENDAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERNDA021545This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEAlcon Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEOLOPATADINE HYDROCHLORIDEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH2 
ACTIVE INGRED UNITmg/mL 
PHARM CLASSESDecreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Histamine-1 Receptor Inhibitor [EPC], Mast Cell Stabilizer [EPC] 

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This page was last updated on: 2/1/2023