69842-302 NDC - ACETAMINOPHEN ()

Drug Information

  • Product NDC: 69842-302
  • Proprietary Name: Acetaminophen
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: CVS PHARMACY, INC
Product Type:
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:11/2/2015
End Marketing Date:3/29/2019

Package Information

No. Package Code Package Description Billing Unit
169842-302-0124 CAPSULE in 1 BOTTLE (69842-302-01)
269842-302-0230 CAPSULE in 1 BOTTLE (69842-302-02)
369842-302-0350 CAPSULE in 1 BOTTLE (69842-302-03)
469842-302-04100 CAPSULE in 1 BOTTLE (69842-302-04)
569842-302-05120 CAPSULE in 1 BOTTLE (69842-302-05)
669842-302-06225 CAPSULE in 1 BOTTLE (69842-302-06)
769842-302-07300 CAPSULE in 1 BOTTLE (69842-302-07)
869842-302-08400 CAPSULE in 1 BOTTLE (69842-302-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC69842-302The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
PROPRIETARY NAMEAcetaminophenThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/2/2015Product 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.
END MARKETING DATE3/29/2019This 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 NAMEOTC MONOGRAPH NOT FINALAn 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.
APPLICATION NUMBERpart343 
LABELER NAMECVS PHARMACY, 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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