NDC 43353-779 Methocarbamol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 43353-779-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-779-53
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-779-60
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-779-70
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-779-80
Package Description: 180 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-779-90
Package Description: 240 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-779-92
Package Description: 270 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-779?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- WATER (UNII: 059QF0KO0R)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STEARIC ACID (UNII: 4ELV7Z65AP)
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".