11673-571 NDC - UP AND UP ALLERGY RELIEF ()

Drug Information

  • Product NDC: 11673-571
  • Proprietary Name: up and up allergy relief
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Target Corporation
Product Type:
FDA Application Number: ANDA076447
Marketing Category: ANDA
Start Marketing Date:4/13/2011

Package Information

No. Package Code Package Description Billing Unit
111673-571-011 BOTTLE in 1 CARTON (11673-571-01) / 70 TABLET, FILM COATED in 1 BOTTLE
211673-571-2215 BLISTER PACK in 1 CARTON (11673-571-22) / 1 TABLET, FILM COATED in 1 BLISTER PACKEA
311673-571-3360 TABLET, FILM COATED in 1 BOTTLE (11673-571-33)
411673-571-391 BOTTLE in 1 CARTON (11673-571-39) / 30 TABLET, FILM COATED in 1 BOTTLEEA
511673-571-471 BOTTLE in 1 CARTON (11673-571-47) / 150 TABLET, FILM COATED in 1 BOTTLE
611673-571-491 BOTTLE in 1 CARTON (11673-571-49) / 40 TABLET, FILM COATED in 1 BOTTLE
711673-571-751 BOTTLE in 1 CARTON (11673-571-75) / 90 TABLET, FILM COATED in 1 BOTTLE
811673-571-762 BOTTLE in 1 CARTON (11673-571-76) / 60 TABLET, FILM COATED in 1 BOTTLE
911673-571-871 BOTTLE in 1 CARTON (11673-571-87) / 300 TABLET, FILM COATED in 1 BOTTLE
1011673-571-951 BOTTLE in 1 CARTON (11673-571-95) / 45 TABLET, FILM COATED in 1 BOTTLEEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC11673-571The 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 NAMEup and up allergy reliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/13/2011This 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 NUMBERANDA076447This 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 NAMETarget CorporationName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/21/2026

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