NDC 17478-151 Rifampin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17478 - Akorn
- 17478-151 - Rifampin
Product Packages
NDC Code 17478-151-42
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE / 10 mL in 1 VIAL
Product Details
What is NDC 17478-151?
What are the uses for Rifampin?
Which are Rifampin UNII Codes?
The UNII codes for the active ingredients in this product are:
- RIFAMPIN (UNII: VJT6J7R4TR)
- RIFAMPIN (UNII: VJT6J7R4TR) (Active Moiety)
Which are Rifampin 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:
- SODIUM FORMALDEHYDE SULFOXYLATE DIHYDRATE (UNII: SQ4705447D)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Rifampin?
- RxCUI: 312821 - rifAMPin 600 MG Injection
- RxCUI: 312821 - rifampin 600 MG Injection
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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".