NDC 55111-641 Meprobamate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55111 - Dr.reddy's Laboratories Limited
- 55111-641 - Meprobamate
Product Characteristics
11 MM
I;4
Product Packages
NDC Code 55111-641-05
Package Description: 500 TABLET in 1 BOTTLE
Product Details
What is NDC 55111-641?
What are the uses for Meprobamate?
Which are Meprobamate UNII Codes?
The UNII codes for the active ingredients in this product are:
- MEPROBAMATE (UNII: 9I7LNY769Q)
- MEPROBAMATE (UNII: 9I7LNY769Q) (Active Moiety)
Which are Meprobamate 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Meprobamate?
- RxCUI: 197928 - meprobamate 200 MG Oral Tablet
- RxCUI: 197929 - meprobamate 400 MG Oral Tablet
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Patient Education
Meprobamate
Meprobamate is used to treat anxiety disorders or for short-term relief of the symptoms of anxiety in adults and children 6 years of age and older. Meprobamate is in a class of medications called tranquilizers. It works by slowing activity in the brain to allow for relaxation.
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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".