NDC 66116-378 Metformin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66116 - Medvantx, Inc.
- 66116-378 - Metformin Hydrochloride
Product Characteristics
Product Packages
NDC Code 66116-378-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 66116-378?
What are the uses for Metformin Hydrochloride?
Which are Metformin Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- METFORMIN HYDROCHLORIDE (UNII: 786Z46389E)
- METFORMIN (UNII: 9100L32L2N) (Active Moiety)
Which are Metformin Hydrochloride 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:
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Metformin Hydrochloride?
- RxCUI: 861004 - metFORMIN HCl 1000 MG Oral Tablet
- RxCUI: 861004 - metformin hydrochloride 1000 MG Oral Tablet
- RxCUI: 861004 - metformin HCl 1 GM Oral Tablet
- RxCUI: 861007 - metFORMIN HCl 500 MG Oral Tablet
- RxCUI: 861007 - metformin hydrochloride 500 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".