NDC 54868-4325 Bactroban
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4325 - Bactroban
Product Characteristics
Product Packages
NDC Code 54868-4325-0
Package Description: 10 CARTON in 1 PACKAGE / 1 TUBE in 1 CARTON / 1 g in 1 TUBE
Product Details
What is NDC 54868-4325?
What are the uses for Bactroban?
Which are Bactroban UNII Codes?
The UNII codes for the active ingredients in this product are:
- MUPIROCIN CALCIUM (UNII: RG38I2P540)
- MUPIROCIN (UNII: D0GX863OA5) (Active Moiety)
Which are Bactroban 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:
- PARAFFIN (UNII: I9O0E3H2ZE)
What is the NDC to RxNorm Crosswalk for Bactroban?
- RxCUI: 108758 - Bactroban 2 % Nasal Ointment
- RxCUI: 108758 - mupirocin 0.02 MG/MG Nasal Ointment [Bactroban]
- RxCUI: 108758 - Bactroban 0.02 MG/MG Nasal Ointment
- RxCUI: 311878 - mupirocin calcium 2 % Nasal Ointment
- RxCUI: 311878 - mupirocin 0.02 MG/MG Nasal Ointment
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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".