47682-075 NDC - LAB SAFETY SUPPLY IBUPROFEN ()

Drug Information

  • Product NDC: 47682-075
  • Proprietary Name: Lab Safety Supply Ibuprofen
  • Non Proprietary Name:
  • Active Ingredient(s): 1.3 mg/mL BENZALKONIUM CHLORIDE
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Unifirst First Aid Corporation
Product Type:
FDA Application Number: ANDA075139
Marketing Category: ANDA
Start Marketing Date:12/30/2008
End Marketing Date:9/27/2012

Package Information

No. Package Code Package Description Billing Unit
147682-075-13500 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (47682-075-13)
247682-075-33100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (47682-075-33)
347682-075-7325 PACKET in 1 CARTON (47682-075-73) / 2.1 mL in 1 PACKET

NDC Record

Field Name Field Value Definition
PRODUCT NDC47682-075The 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 NAMELab Safety Supply IbuprofenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/30/2008This 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 NUMBERANDA075139This 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 NAMEUnifirst First Aid CorporationName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC47682-075The 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 NAMEGreen Guard Antiseptic WipesThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/1/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBERM003This 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 NAMEUniFirst First Aid CorporationName of Company corresponding to the labeler code segment of the Product NDC.

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

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