NDC 17856-3728 Propranolol Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corp.
- 17856-3728 - Propranolol Hydrochloride
Product Packages
NDC Code 17856-3728-1
Package Description: 72 CUP in 1 CASE / 5 mL in 1 CUP
Product Details
What is NDC 17856-3728?
What are the uses for Propranolol Hydrochloride?
Which are Propranolol Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROPRANOLOL HYDROCHLORIDE (UNII: F8A3652H1V)
- PROPRANOLOL (UNII: 9Y8NXQ24VQ) (Active Moiety)
Which are Propranolol 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:
- ALCOHOL (UNII: 3K9958V90M)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Propranolol Hydrochloride?
- RxCUI: 856724 - propranolol HCl 20 MG in 5 mL Oral Solution
- RxCUI: 856724 - propranolol hydrochloride 4 MG/ML Oral Solution
- RxCUI: 856724 - propranolol hydrochloride 20 MG per 5 ML Oral Solution
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Patient Education
Propranolol (Infantile Hemangioma)
Propranolol oral solution is used to treat proliferating infantile hemangioma (benign [noncancerous] growths or tumors appearing on or under the skin shortly after birth) in infants 5 weeks to 5 months of age. Propranolol is in a class of medications called beta blockers. It works by narrowing the blood vessels already formed and by preventing new ones from growing.
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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".