0023-3616 NDC - LATISSE (BIMATOPROST)

Drug Information

Product NDC: 0023-3616

Proprietary Name: LATISSE

Non Proprietary Name: bimatoprost

Active Ingredient(s):
  • .3 mg/mL BIMATOPROST


Administration Route(s): OPHTHALMIC

Dosage Form(s): SOLUTION/ DROPS

Pharmacy Class(es):
  • Prostaglandin Analog [EPC];
  • Prostaglandins [CS]

Labeler Information

Labeler Name: Allergan, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022369
Marketing Category: NDA
Start Marketing Date:1/26/2009

Package Information

No. Package Code Package Description Billing Unit
10023-3616-031 BOTTLE, DROPPER in 1 CARTON (0023-3616-03) > 3 mL in 1 BOTTLE, DROPPERML
20023-3616-041 BOTTLE, DROPPER in 1 CARTON (0023-3616-04) > 3 mL in 1 BOTTLE, DROPPER
30023-3616-051 BOTTLE, DROPPER in 1 CARTON (0023-3616-05) > 5 mL in 1 BOTTLE, DROPPERML
40023-3616-161 BOTTLE, DROPPER in 1 CARTON (0023-3616-16) > 1.5 mL in 1 BOTTLE, DROPPER
50023-3616-701 BOTTLE, DROPPER in 1 CARTON (0023-3616-70) > 3 mL in 1 BOTTLE, DROPPERML
60023-3616-711 BOTTLE, DROPPER in 1 CARTON (0023-3616-71) > 3 mL in 1 BOTTLE, DROPPER
70023-3616-801 BOTTLE, DROPPER in 1 CARTON (0023-3616-80) > 3 mL in 1 BOTTLE, DROPPERML
80023-3616-811 BOTTLE, DROPPER in 1 CARTON (0023-3616-81) > 3 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC0023-3616The 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 NAMELATISSEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEbimatoprostThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTION/ DROPSThe 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 DATE1/26/2009This 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 NUMBERNDA022369This 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 NAMEAllergan, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEBIMATOPROSTThe following is the list of active ingredients in this product. An 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 STRENGTH.3 
ACTIVE INGRED UNITmg/mL 
PHARM CLASSESProstaglandin Analog [EPC], Prostaglandins [CS] 

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This page was last updated on: 9/15/2022