NDC 71205-983 Salsalate

Tablet, Film Coated Oral - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
71205-983
Proprietary Name:
Salsalate
Non-Proprietary Name: [1]
Salsalate
Substance Name: [2]
Salsalate
NDC Directory Status:
Human Prescription Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Proficient Rx Lp
    Labeler Code:
    71205
    Marketing Category: [8]
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date: [9]
    08-24-2017
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

    Color(s):
    YELLOW (C48330)
    Shape:
    ROUND (C48348)
    OVAL (C48345)
    Size(s):
    11 MM
    80 MM
    Imprint(s):
    809
    810
    Score:
    1
    2

    Product Packages

    NDC Code 71205-983-00

    Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    NDC Code 71205-983-11

    Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    NDC Code 71205-983-30

    Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    NDC Code 71205-983-55

    Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    NDC Code 71205-983-60

    Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    NDC Code 71205-983-72

    Package Description: 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    NDC Code 71205-983-90

    Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    Product Details

    What is NDC 71205-983?

    The NDC code 71205-983 is assigned by the FDA to the product Salsalate which is a human prescription drug product labeled by Proficient Rx Lp. The product's dosage form is tablet, film coated and is administered via oral form. The product is distributed in 7 packages with assigned NDC codes 71205-983-00 100 tablet, film coated in 1 bottle, plastic , 71205-983-11 1000 tablet, film coated in 1 bottle, plastic , 71205-983-30 30 tablet, film coated in 1 bottle, plastic , 71205-983-55 500 tablet, film coated in 1 bottle, plastic , 71205-983-60 60 tablet, film coated in 1 bottle, plastic , 71205-983-72 120 tablet, film coated in 1 bottle, plastic , 71205-983-90 90 tablet, film coated in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Salsalate?

    Salsalate is used to relieve pain from various conditions. It also reduces pain, swelling, and joint stiffness from arthritis. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID).

    What are Salsalate Active Ingredients?

    An 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.

    Which are Salsalate UNII Codes?

    The UNII codes for the active ingredients in this product are:

    What is the NDC to RxNorm Crosswalk for Salsalate?

    RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

    * Please review the disclaimer below.

    Patient Education

    Salsalate


    Salsalate is used to relieve pain, tenderness, swelling, and stiffness caused by rheumatoid arthritis (arthritis caused by swelling of the lining of the joints), osteoarthritis (arthritis caused by a breakdown of the lining of the joints), and other conditions that cause swelling. Salsalate is in a class of nonsteroidal anti-inflammatory medications (NSAIDs) called salicylates. It works by stopping the body's production of a substance that causes pain, fever, and swelling.
    [Learn More]


    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An 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.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".