NDC 33261-600 Amoxicillin And Clavulanate Potassium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-600 - Amoxicillin And Clavulanate Potassium
Product Characteristics
Product Packages
NDC Code 33261-600-01
Package Description: 75 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-600?
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)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ASPARTAME (UNII: Z0H242BBR1)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
What is the NDC to RxNorm Crosswalk for Amoxicillin And Clavulanate Potassium?
- RxCUI: 617993 - amoxicillin 600 MG / clavulanic acid 42.9 MG in 5 mL Oral Suspension
- RxCUI: 617993 - amoxicillin 120 MG/ML / clavulanate 8.58 MG/ML Oral Suspension
- RxCUI: 617993 - amoxicillin (as amoxicillin trihydrate) 600 MG / clavulanic acid (as clavulanate potassium) 42.9 MG per 5 ML Oral Suspension
- RxCUI: 617993 - amoxicillin 600 MG / clavulanic acid 42.9 MG per 5 ML Oral Suspension
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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".