0517-0830 NDC - LATANOPROST

Drug Information

Product NDC: 0517-0830

Proprietary Name: Latanoprost

Non Proprietary Name: Latanoprost

Active Ingredient(s):
  • 50 ug/mL LATANOPROST


Administration Route(s): OPHTHALMIC

Dosage Form(s): SOLUTION

Pharmacy Class(es):
  • Prostaglandin Analog [EPC];
  • Prostaglandins [Chemical/Ingredient]

Labeler Information

Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200925
Marketing Category: ANDA
Start Marketing Date:8/2/2011

Package Information

No. Package Code Package Description Billing Unit
10517-0830-011 BOTTLE, PLASTIC in 1 CARTON (0517-0830-01) > 2.5 mL in 1 BOTTLE, PLASTICML
20517-0830-031 BOTTLE, PLASTIC in 1 CARTON (0517-0830-03) > 2.5 mL in 1 BOTTLE, PLASTIC

NDC Record

Field Name Field Value Definition
PRODUCT NDC0517-0830The 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 PRESCRIPTION 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 NAMELatanoprostThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMELatanoprostThe 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 DATE8/2/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct 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 NUMBERANDA200925This 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 NAMEAmerican Regent, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMELATANOPROSTThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH50 
ACTIVE INGRED UNITug/mL 
PHARM CLASSESProstaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] 

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This page was last updated on: 7/15/2019