NDC 21695-464 Levaquin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-464 - Levaquin
Product Characteristics
Product Packages
NDC Code 21695-464-07
Package Description: 7 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 21695-464?
What are the uses for Levaquin?
Which are Levaquin UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOFLOXACIN (UNII: 6GNT3Y5LMF)
- LEVOFLOXACIN (UNII: 6GNT3Y5LMF) (Active Moiety)
Which are Levaquin 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:
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CROSPOVIDONE (UNII: 68401960MK)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Levaquin?
- RxCUI: 199885 - levoFLOXacin 500 MG Oral Tablet
- RxCUI: 199885 - levofloxacin 500 MG Oral Tablet
- RxCUI: 211816 - LEVAQUIN 500 MG Oral Tablet
- RxCUI: 211816 - levofloxacin 500 MG Oral Tablet [Levaquin]
- RxCUI: 211816 - Levaquin 500 MG Oral Tablet
* 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".