NDC 33261-876 Levofloxacin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-876 - Levofloxacin
Product Characteristics
ORANGE (C48331 - PEACH)
WHITE (C48325 - WHITE)
18 MM
22 MM
W;545
W;547
Product Packages
NDC Code 33261-876-10
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-876-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-876?
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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POVIDONES (UNII: FZ989GH94E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Levofloxacin?
- RxCUI: 199884 - levoFLOXacin 250 MG Oral Tablet
- RxCUI: 199884 - levofloxacin 250 MG Oral Tablet
- RxCUI: 199884 - levofloxacin (as levofloxacin hemihydrate) 250 MG Oral Tablet
- RxCUI: 199885 - levoFLOXacin 500 MG Oral Tablet
- RxCUI: 199885 - levofloxacin 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".