NDC 54868-0586 Methocarbamol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-0586 - Methocarbamol
Product Characteristics
Product Packages
NDC Code 54868-0586-2
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 54868-0586-3
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 54868-0586-6
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 54868-0586-7
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 54868-0586-8
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 54868-0586?
What are the uses for Methocarbamol?
Which are Methocarbamol UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHOCARBAMOL (UNII: 125OD7737X)
- METHOCARBAMOL (UNII: 125OD7737X) (Active Moiety)
Which are Methocarbamol 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:
- METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- STARCH, CORN (UNII: O8232NY3SJ)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Methocarbamol?
- RxCUI: 197943 - methocarbamol 500 MG Oral Tablet
- RxCUI: 197944 - methocarbamol 750 MG Oral Tablet
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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".