NDC 52959-026 Carisoprodol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52959 - H.j. Harkins Company, Inc.
- 52959-026 - Carisoprodol
Product Characteristics
Product Packages
NDC Code 52959-026-00
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-03
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-06
Package Description: 6 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-10
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-12
Package Description: 12 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-14
Package Description: 14 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-15
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-20
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-21
Package Description: 21 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-24
Package Description: 24 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-25
Package Description: 25 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-28
Package Description: 28 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-32
Package Description: 32 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-40
Package Description: 40 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-42
Package Description: 42 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-45
Package Description: 45 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-50
Package Description: 50 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-52
Package Description: 52 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-56
Package Description: 56 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-80
Package Description: 80 TABLET in 1 BOTTLE, PLASTIC
NDC Code 52959-026-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 52959-026?
What are the uses for Carisoprodol?
Which are Carisoprodol UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARISOPRODOL (UNII: 21925K482H)
- CARISOPRODOL (UNII: 21925K482H) (Active Moiety)
Which are Carisoprodol 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POVIDONE K30 (UNII: U725QWY32X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J)
What is the NDC to RxNorm Crosswalk for Carisoprodol?
- RxCUI: 197446 - carisoprodol 350 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Pseudoephedrine
Pseudoephedrine is used to relieve nasal congestion caused by colds, allergies, and hay fever. It is also used to temporarily relieve sinus congestion and pressure. Pseudoephedrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Pseudoephedrine is in a class of medications called nasal decongestants. It works by causing narrowing of the blood vessels in the nasal passages.
[Learn More]
Carisoprodol
Carisoprodol is used with rest, physical therapy, and other measures to relax muscles and relieve pain and discomfort caused by strains, sprains, and other muscle injuries. Carisoprodol is in a class of medications called skeletal muscle relaxants. It works by acting in the brain and nervous system to allow the muscles to relax.
[Learn More]
Betamethasone Topical
Betamethasone topical is used to treat the itching, redness, dryness, crusting, scaling, inflammation, and discomfort of various skin conditions, including psoriasis (a skin disease in which red, scaly patches form on some areas of the body) and eczema (a skin disease that causes the skin to be dry and itchy and to sometimes develop red, scaly rashes). Betamethasone is in a class of medications called corticosteroids. It works by activating natural substances in the skin to reduce swelling, redness, and itching.
[Learn More]
Steroids
You may have heard of anabolic steroids, which can have harmful effects. But there's another type of steroid - sometimes called a corticosteroid - that treats a variety of problems. These steroids are similar to hormones that your adrenal glands make to fight stress associated with illnesses and injuries. They reduce inflammation and affect the immune system.
You may need to take corticosteroids to treat:
- Arthritis
- Asthma
- Autoimmune diseases such as lupus and multiple sclerosis
- Skin conditions such as eczema and rashes
- Some kinds of cancer
Steroids are strong medicines, and they can have side effects, including weakened bones and cataracts. Because of this, you usually take them for as short a time as possible.
[Learn More]
* 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".