NDC 43353-842 Metformin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Llc
- 43353-842 - Metformin Hydrochloride
Product Characteristics
Product Packages
NDC Code 43353-842-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-842-53
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-842-60
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-842-70
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-842-80
Package Description: 180 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-842-92
Package Description: 270 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-842-94
Package Description: 360 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-842-96
Package Description: 450 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-842?
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:
- POVIDONE (UNII: FZ989GH94E)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TALC (UNII: 7SEV7J4R1U)
- ACACIA (UNII: 5C5403N26O)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
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
* 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".