NDC 53217-406 Cefdinir
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53217 - Aidarex Pharmaceuticals Llc
- 53217-406 - Cefdinir
Product Characteristics
Product Packages
NDC Code 53217-406-01
Package Description: 100 mL in 1 BOTTLE
Product Details
What is NDC 53217-406?
What are the uses for Cefdinir?
Which are Cefdinir UNII Codes?
The UNII codes for the active ingredients in this product are:
- CEFDINIR MONOHYDRATE (UNII: 6E7SN358SE)
- CEFDINIR (UNII: CI0FAO63WC) (Active Moiety)
Which are Cefdinir 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GUAR GUM (UNII: E89I1637KE)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ANHYDROUS TRISODIUM CITRATE (UNII: RS7A450LGA)
- SUCROSE (UNII: C151H8M554)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Cefdinir?
- RxCUI: 476576 - cefdinir 250 MG in 5 mL Oral Suspension
- RxCUI: 476576 - cefdinir 50 MG/ML Oral Suspension
- RxCUI: 476576 - cefdinir 250 MG per 5 ML Oral Suspension
* 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".