NDC 17856-0286 Levofloxacin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BUBBLE GUM (C73368 - ARTIFICIAL FLAVOR)
Code Structure Chart
Product Details
What is NDC 17856-0286?
What are the uses for Levofloxacin?
Which are Levofloxacin UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOFLOXACIN (UNII: 6GNT3Y5LMF)
- LEVOFLOXACIN ANHYDROUS (UNII: RIX4E89Y14) (Active Moiety)
Which are Levofloxacin 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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SUCROSE (UNII: C151H8M554)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GRAPE (UNII: 6X543N684K)
What is the NDC to RxNorm Crosswalk for Levofloxacin?
- RxCUI: 477391 - levoFLOXacin 25 MG in 1 mL Oral Solution
- RxCUI: 477391 - levofloxacin 25 MG/ML Oral Solution
- RxCUI: 477391 - levofloxacin 25 MG per 1 ML Oral Solution
- RxCUI: 477391 - levofloxacin 250 MG per 10 ML Oral Solution
- RxCUI: 477391 - levofloxacin 500 MG per 20 ML Oral Solution
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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".