NDC 43353-936 Metformin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Llc
- 43353-936 - Metformin Hydrochloride
Product Characteristics
OVAL (C48345)
19 MM
E;221
Product Packages
NDC Code 43353-936-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-936-45
Package Description: 45 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-936-53
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-936-60
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-936-73
Package Description: 135 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-936-80
Package Description: 180 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-936-86
Package Description: 225 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-936?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONE K12 (UNII: 333AG72FWJ)
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".