NDC 17856-3755 Furosemide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-3755 - Furosemide
Product Packages
NDC Code 17856-3755-1
Package Description: 240 mL in 1 CUP
Product Details
What is NDC 17856-3755?
What are the uses for Furosemide?
Which are Furosemide UNII Codes?
The UNII codes for the active ingredients in this product are:
- FUROSEMIDE (UNII: 7LXU5N7ZO5)
- FUROSEMIDE (UNII: 7LXU5N7ZO5) (Active Moiety)
Which are Furosemide 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:
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITOL (UNII: 506T60A25R)
- WATER O-15 (UNII: 63M8RYN44N)
What is the NDC to RxNorm Crosswalk for Furosemide?
- RxCUI: 197731 - furosemide 40 MG in 5 mL Oral Solution
- RxCUI: 197731 - furosemide 8 MG/ML Oral Solution
- RxCUI: 197731 - furosemide 40 MG per 5 ML Oral Solution
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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".