NDC 31722-339 Naproxen Delayed Release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 31722 - Camber Pharmaceuticals
- 31722-339 - Naproxen
Product Characteristics
16 MM
I;11
Product Packages
NDC Code 31722-339-05
Package Description: 24 BOTTLE in 1 CASE / 100 TABLET in 1 BOTTLE (31722-339-01)
Price per Unit: $0.18986 per EA
NDC Code 31722-339-50
Package Description: 12 BOTTLE in 1 CASE / 500 TABLET in 1 BOTTLE (31722-339-10)
Product Details
What is NDC 31722-339?
What are the uses for Naproxen Delayed Release?
Which are Naproxen Delayed Release UNII Codes?
The UNII codes for the active ingredients in this product are:
- NAPROXEN (UNII: 57Y76R9ATQ)
- NAPROXEN (UNII: 57Y76R9ATQ) (Active Moiety)
Which are Naproxen Delayed Release Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Naproxen Delayed Release?
- RxCUI: 311915 - naproxen 500 MG Delayed Release Oral Tablet
- RxCUI: 311915 - naproxen (as naproxen sodium) 500 MG Delayed Release Oral Tablet
- RxCUI: 603103 - naproxen 375 MG Delayed Release Oral Tablet
- RxCUI: 603103 - naproxen 375 MG (as naproxen sodium 413 MG) Delayed Release Oral Tablet
* Please review the disclaimer below.
Patient Education
Naproxen
Prescription naproxen is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints), rheumatoid arthritis (arthritis caused by swelling of the lining of the joints), juvenile arthritis (a form of joint disease in children), and ankylosing spondylitis (arthritis that mainly affects the spine). Prescription naproxen tablets, extended-release tablets, and suspension are also used to relieve shoulder pain caused by bursitis (inflammation of a fluid-filled sac in the shoulder joint), tendinitis (inflammation of the tissue that connects muscle to bone), gouty arthritis (attacks of joint pain caused by a build-up of certain substances in the joints), and pain from other causes, including menstrual pain (pain that happens before or during a menstrual period). Nonprescription naproxen is used to reduce fever and to relieve mild pain from headaches, muscle aches, arthritis, menstrual periods, the common cold, toothaches, and backaches. Naproxen is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.
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Pain Relievers
Pain relievers are medicines that reduce or relieve headaches, sore muscles, arthritis, or other aches and pains. There are many different pain medicines, and each one has advantages and risks. Some types of pain respond better to certain medicines than others. Each person may also have a slightly different response to a pain reliever.
Over-the-counter (OTC) medicines are good for many types of pain. There are two main types of OTC pain medicines: acetaminophen (Tylenol) and nonsteroidal anti-inflammatory drugs (NSAIDs). Aspirin, naproxen (Aleve), and ibuprofen (Advil, Motrin) are examples of OTC NSAIDs.
If OTC medicines don't relieve your pain, your doctor may prescribe something stronger. Many NSAIDs are also available at higher prescription doses. The most powerful pain relievers are opioids. They are very effective, but they can sometimes have serious side effects. There is also a risk of addiction. Because of the risks, you must use them only under a doctor's supervision.
There are many things you can do to help ease pain. Pain relievers are just one part of a pain treatment plan.
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* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".