NDC 54868-5938 Azithromycin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5938 - Azithromycin
Product Characteristics
BANANA (C73364)
Product Packages
NDC Code 54868-5938-0
Package Description: 3 POWDER, FOR SUSPENSION in 1 BOX
Product Details
What is NDC 54868-5938?
What are the uses for Azithromycin?
Which are Azithromycin UNII Codes?
The UNII codes for the active ingredients in this product are:
- AZITHROMYCIN DIHYDRATE (UNII: 5FD1131I7S)
- 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM PHOSPHATE, TRIBASIC ANHYDROUS (UNII: SX01TZO3QZ)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Azithromycin?
- RxCUI: 861416 - azithromycin 1 GM Powder for Oral Suspension
- RxCUI: 861416 - azithromycin 1000 MG Powder for 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".