67751-144 NDC - ALEVE ()

Drug Information

  • Product NDC: 67751-144
  • Proprietary Name: Aleve
  • Non Proprietary Name:
  • Active Ingredient(s): 220 mg/1 NAPROXEN SODIUM
  • Administration Route(s):
  • Dosage Form(s):
  • Pharmacy Class(es): Anti-Inflammatory Agents; Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Navajo Manufacturing Company Inc.
Product Type:
FDA Application Number: NDA020204
Marketing Category: NDA
Start Marketing Date:9/17/2016
End Marketing Date:9/18/2016

Package Information

No. Package Code Package Description Billing Unit
167751-144-011 POUCH in 1 CARTON (67751-144-01) / 1 TABLET in 1 POUCH
267751-144-021 POUCH in 1 CARTON (67751-144-02) / 2 TABLET in 1 POUCH
367751-144-031 POUCH in 1 CARTON (67751-144-03) / 1 TABLET in 1 POUCH
467751-144-042 POUCH in 1 CARTON (67751-144-04) / 1 TABLET in 1 POUCH
567751-144-0512 POUCH in 1 TRAY (67751-144-05) / 1 TABLET in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC67751-144The 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 NAMEAleveThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/17/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
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 NUMBERNDA020204This 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 NAMENavajo Manufacturing Company Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC67751-144The 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 NAMEAleveThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/4/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
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 NUMBERNDA020204This 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 NAMENavajo Manufacturing Company 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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