16714-351 NDC - FLUOXETINE

Drug Information

Product NDC: 16714-351

Proprietary Name: Fluoxetine

Non Proprietary Name: Fluoxetine

Active Ingredient(s):
  • 10 mg/1 FLUOXETINE HYDROCHLORIDE


Administration Route(s): ORAL

Dosage Form(s): CAPSULE

Pharmacy Class(es):
  • Serotonin Reuptake Inhibitor [EPC];
  • Serotonin Uptake Inhibitors [MoA]

Labeler Information

Labeler Name: NorthStar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090223
Marketing Category: ANDA
Start Marketing Date:7/1/2009

Package Information

No. Package Code Package Description Billing Unit
116714-351-0130 CAPSULE in 1 BOTTLE (16714-351-01)EA
216714-351-021000 CAPSULE in 1 BOTTLE (16714-351-02)EA
316714-351-03100 CAPSULE in 1 BOTTLE (16714-351-03)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC16714-351The 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 NAMEFluoxetineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEFluoxetineThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECAPSULEThe 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 DATE7/1/2009This 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 NUMBERANDA090223This 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 NAMENorthStar RxLLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEFLUOXETINE HYDROCHLORIDEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH10 
ACTIVE INGRED UNITmg/1 
PHARM CLASSESSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] 

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This page was last updated on: 5/17/2019