NDC 67296-0716 Amoxicillin And Clavulanate Potassium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67296 - Redpharm Drug Inc.
- 67296-0716 - Amoxicillin And Clavulanate Potassium
Product Characteristics
Product Packages
NDC Code 67296-0716-1
Package Description: 14 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 67296-0716?
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 (UNII: 804826J2HU) (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)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CROSPOVIDONE (UNII: 68401960MK)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
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
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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".