NDC 71205-983 Salsalate
Tablet, Film Coated Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
OVAL (C48345)
80 MM
810
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?
What are the uses for Salsalate?
What are Salsalate Active Ingredients?
Which are Salsalate UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALSALATE (UNII: V9MO595C9I)
- SALSALATE (UNII: V9MO595C9I) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Salsalate?
- RxCUI: 312899 - salsalate 500 MG Oral Tablet
- RxCUI: 583170 - salsalate 750 MG Oral Tablet
* 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.
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* Please review the disclaimer below.
[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".