NDC 17478-526 Bal
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17478 - Akorn
- 17478-526 - Bal
Product Packages
NDC Code 17478-526-03
Package Description: 10 AMPULE in 1 CARTON / 3 mL in 1 AMPULE
Product Details
What is NDC 17478-526?
What are the uses for Bal?
Which are Bal UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMERCAPROL (UNII: 0CPP32S55X)
- DIMERCAPROL (UNII: 0CPP32S55X) (Active Moiety)
Which are Bal 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:
- BENZYL BENZOATE (UNII: N863NB338G)
- PEANUT OIL (UNII: 5TL50QU0W4)
What is the NDC to RxNorm Crosswalk for Bal?
- RxCUI: 208325 - BAL in Oil 100 MG/ML in 3 ML Injection
- RxCUI: 208325 - 3 ML dimercaprol 100 MG/ML Injection [BAL in Oil]
- RxCUI: 208325 - BAL in Oil 100 MG/ML per 3 ML Injection
- RxCUI: 309915 - dimercaprol 100 MG/ML in 3 ML Injection
- RxCUI: 309915 - 3 ML dimercaprol 100 MG/ML 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".