52584-102 NDC - FUROSEMIDE ()

Drug Information

  • Product NDC: 52584-102
  • Proprietary Name: Furosemide
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: General Injectables & Vaccines, Inc
Product Type:
FDA Application Number: NDA018667
Marketing Category: NDA
Start Marketing Date:8/1/2010

Package Information

No. Package Code Package Description Billing Unit
152584-102-021 VIAL, SINGLE-DOSE in 1 BAG (52584-102-02) / 2 mL in 1 VIAL, SINGLE-DOSE
252584-102-041 VIAL, SINGLE-DOSE in 1 BAG (52584-102-04) / 4 mL in 1 VIAL, SINGLE-DOSE
352584-102-101 VIAL, SINGLE-DOSE in 1 BAG (52584-102-10) / 10 mL in 1 VIAL, SINGLE-DOSE

NDC Record

Field Name Field Value Definition
PRODUCT NDC52584-102The 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.
PROPRIETARY NAMEFurosemideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/1/2010This 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 NUMBERNDA018667This 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 NAMEGeneral Injectables & Vaccines, IncName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/4/2025

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