NDC 54868-5217 Metformin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5217 - Metformin Hydrochloride
Product Characteristics
Product Packages
NDC Code 54868-5217-0
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-5217-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-5217-2
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-5217-3
Package Description: 180 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-5217-4
Package Description: 120 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-5217-5
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-5217?
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:
- XANTHAN GUM (UNII: TTV12P4NEE)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- POVIDONE (UNII: FZ989GH94E)
- TALC (UNII: 7SEV7J4R1U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for Metformin Hydrochloride?
- RxCUI: 860975 - metFORMIN HCl 500 MG 24HR Extended Release Oral Tablet
- RxCUI: 860975 - 24 HR metformin hydrochloride 500 MG Extended Release Oral Tablet
- RxCUI: 860975 - metformin HCl 500 MG 24 HR Extended Release Oral Tablet
- RxCUI: 860981 - metFORMIN HCl 750 MG 24HR Extended Release Oral Tablet
- RxCUI: 860981 - 24 HR metformin hydrochloride 750 MG Extended Release Oral Tablet
* Please review the disclaimer below.
[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".