0093-0711 NDC - FLURBIPROFEN

Drug Information

Product NDC: 0093-0711

Proprietary Name: Flurbiprofen

Non Proprietary Name: Flurbiprofen

Active Ingredient(s):
  • 100 mg/1 FLURBIPROFEN


Administration Route(s): ORAL

Dosage Form(s): TABLET, FILM COATED

Pharmacy Class(es):
  • Cyclooxygenase Inhibitors [MoA];
  • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient];
  • Nonsteroidal Anti-inflammatory Drug [EPC]

Labeler Information

Labeler Name: Teva Pharmaceuticals USA, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074431
Marketing Category: ANDA
Start Marketing Date:6/2/1995

Package Information

No. Package Code Package Description Billing Unit
10093-0711-01100 TABLET, FILM COATED in 1 BOTTLE (0093-0711-01)EA
20093-0711-05500 TABLET, FILM COATED in 1 BOTTLE (0093-0711-05)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC0093-0711The 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 NAMEFlurbiprofenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEFlurbiprofenThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLET, FILM COATEDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE6/2/1995This 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 NUMBERANDA074431This 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 NAMETeva Pharmaceuticals USA, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEFLURBIPROFENThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH100 
ACTIVE INGRED UNITmg/1 
PHARM CLASSESCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] 

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This page was last updated on: 8/16/2019