59779-368 NDC - ALL DAY PAIN RELIEF ()

Drug Information

  • Product NDC: 59779-368
  • Proprietary Name: All Day Pain Relief
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: CVS Pharmacy
Product Type:
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date:1/23/1997
End Marketing Date:8/11/2017

Package Information

No. Package Code Package Description Billing Unit
159779-368-371 BOTTLE in 1 CARTON (59779-368-37) / 270 TABLET, FILM COATED in 1 BOTTLE
259779-368-621 BOTTLE in 1 CARTON (59779-368-62) / 24 TABLET, FILM COATED in 1 BOTTLEEA
359779-368-711 BOTTLE in 1 CARTON (59779-368-71) / 50 TABLET, FILM COATED in 1 BOTTLEEA
459779-368-721 BOTTLE in 1 CARTON (59779-368-72) / 60 TABLET, FILM COATED in 1 BOTTLE
559779-368-821 BOTTLE in 1 CARTON (59779-368-82) / 200 TABLET, FILM COATED in 1 BOTTLEEA
659779-368-90500 TABLET, FILM COATED in 1 BOTTLE (59779-368-90)

NDC Record

Field Name Field Value Definition
PRODUCT NDC59779-368Product 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.
PROPRIETARY NAMEAll Day Pain ReliefThis 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.
START MARKETING DATE1/23/1997Name of Company corresponding to the labeler code segment of the Product NDC.
END MARKETING DATE8/11/2017An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
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 NUMBERANDA074661This 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 NAMECVS PharmacyName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 1/16/2026

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