NDC 53217-263 Azithromycin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53217 - Aidarex Pharmaceuticals Llc
- 53217-263 - Azithromycin
Product Characteristics
Product Packages
NDC Code 53217-263-01
Package Description: 1 BLISTER PACK in 1 CARTON / 6 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 53217-263?
What are the uses for Azithromycin?
Which are Azithromycin UNII Codes?
The UNII codes for the active ingredients in this product are:
- AZITHROMYCIN MONOHYDRATE (UNII: JTE4MNN1MD)
- AZITHROMYCIN ANHYDROUS (UNII: J2KLZ20U1M) (Active Moiety)
Which are Azithromycin 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Azithromycin?
- RxCUI: 248656 - azithromycin 500 MG Oral Tablet
- RxCUI: 248656 - azithromycin 500 MG (as azithromycin monohydrate) Oral Tablet
- RxCUI: 308460 - azithromycin 250 MG Oral Tablet
- RxCUI: 749783 - {6 (azithromycin 250 MG Oral Tablet) } Pack
- RxCUI: 749783 - azithromycin 250 MG Oral Tablet 6 Count Pack
* 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".