50580-112 NDC - TYLENOL ARTHRITIS PAIN ()

Drug Information

  • Product NDC: 50580-112
  • Proprietary Name: Tylenol Arthritis Pain
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: McNeil Consumer Healthcare Div McNeil-PPC, Inc
Product Type:
FDA Application Number: NDA019872
Marketing Category: NDA
Start Marketing Date:12/1/1998
End Marketing Date:11/30/2014

Package Information

No. Package Code Package Description Billing Unit
150580-112-0234 POUCH in 1 CARTON (50580-112-02) / 2 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (50580-112-22)
250580-112-063 POUCH in 1 CARTON (50580-112-06) / 2 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (50580-112-22)EA
350580-112-101 BOTTLE in 1 CARTON (50580-112-10) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
450580-112-121 BOTTLE in 1 CARTON (50580-112-12) / 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLEEA
550580-112-151 BOTTLE in 1 CARTON (50580-112-15) / 150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLEEA
650580-112-21100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50580-112-21)EA
750580-112-222 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (50580-112-22)
850580-112-241 BOTTLE in 1 CARTON (50580-112-24) / 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLEEA
950580-112-251 BOTTLE in 1 CARTON (50580-112-25) / 250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLEEA
1050580-112-291 BOTTLE in 1 CARTON (50580-112-29) / 290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLEEA
1150580-112-371 BOTTLE in 1 CARTON (50580-112-37) / 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLEEA
1250580-112-501 BOTTLE in 1 CARTON (50580-112-50) / 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLEEA
1350580-112-591 BOTTLE in 1 CARTON (50580-112-59) / 190 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC50580-112The 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 NAMETylenol Arthritis PainThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/1/1998This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE11/30/2014This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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 NUMBERNDA019872This 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 NAMEMcNeil Consumer Healthcare Div McNeil-PPC, IncName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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