NDC 17478-420 Labetalol Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17478 - Akorn
- 17478-420 - Labetalol Hydrochloride
Product Packages
NDC Code 17478-420-20
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX / 20 mL in 1 VIAL, MULTI-DOSE
NDC Code 17478-420-40
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX / 40 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 17478-420?
What are the uses for Labetalol Hydrochloride?
Which are Labetalol Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- LABETALOL HYDROCHLORIDE (UNII: 1GEV3BAW9J)
- LABETALOL (UNII: R5H8897N95) (Active Moiety)
Which are Labetalol Hydrochloride 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:
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Labetalol Hydrochloride?
- RxCUI: 896771 - labetalol HCl 5 MG/ML Injectable Solution
- RxCUI: 896771 - labetalol hydrochloride 5 MG/ML Injectable Solution
* Please review the disclaimer below.
[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".