NDC 54868-1385 Cephalexin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 54868-1385?
What are the uses for Cephalexin?
Which are Cephalexin UNII Codes?
The UNII codes for the active ingredients in this product are:
- CEPHALEXIN (UNII: OBN7UDS42Y)
- CEPHALEXIN ANHYDROUS (UNII: 5SFF1W6677) (Active Moiety)
Which are Cephalexin 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)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- SUCROSE (UNII: C151H8M554)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Cephalexin?
- RxCUI: 309110 - cephalexin 125 MG in 5 mL Oral Suspension
- RxCUI: 309110 - cephalexin 25 MG/ML Oral Suspension
- RxCUI: 309110 - cefalexin 25 MG/ML Oral Suspension
- RxCUI: 309110 - cephalexin 125 MG per 5 ML Oral Suspension
- RxCUI: 309113 - cephalexin 250 MG in 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".