NDC 33261-111 Amoxicillin And Clavulanate Potassium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
22 MM
93;22;75
2
Code Structure Chart
Product Details
What is NDC 33261-111?
What are the uses for Amoxicillin And Clavulanate Potassium?
Which are Amoxicillin And Clavulanate Potassium UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMOXICILLIN (UNII: 804826J2HU)
- AMOXICILLIN ANHYDROUS (UNII: 9EM05410Q9) (Active Moiety)
- CLAVULANATE POTASSIUM (UNII: Q42OMW3AT8)
- CLAVULANIC ACID (UNII: 23521W1S24) (Active Moiety)
Which are Amoxicillin And Clavulanate Potassium 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)
- HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)
- HYPROMELLOSE 2910 (50 MPA.S) (UNII: 1IVH67816N)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Amoxicillin And Clavulanate Potassium?
- RxCUI: 562508 - amoxicillin 875 MG / clavulanate potassium 125 MG Oral Tablet
- RxCUI: 562508 - amoxicillin 875 MG / clavulanate 125 MG Oral Tablet
- RxCUI: 562508 - amoxicillin (as amoxicillin trihydrate) 875 MG / clavulanic acid (as clavulanate potassium) 125 MG Oral Tablet
- RxCUI: 617296 - amoxicillin 500 MG / clavulanate potassium 125 MG Oral Tablet
- RxCUI: 617296 - amoxicillin 500 MG / clavulanate 125 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".