NDC 50090-0316 Chlorzoxazone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-0316 - Chlorzoxazone
Product Characteristics
Product Packages
NDC Code 50090-0316-0
Package Description: 7 TABLET in 1 BOTTLE
Product Details
What is NDC 50090-0316?
What are the uses for Chlorzoxazone?
Which are Chlorzoxazone UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORZOXAZONE (UNII: H0DE420U8G)
- CHLORZOXAZONE (UNII: H0DE420U8G) (Active Moiety)
Which are Chlorzoxazone 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:
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Chlorzoxazone?
- RxCUI: 197502 - chlorzoxazone 500 MG Oral Tablet
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Patient Education
Chlorzoxazone
Chlorzoxazone is used to relieve pain and stiffness caused by muscle strains and sprains. It is used in combination with physical therapy, analgesics (such as aspirin or acetaminophen), and rest.
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[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".