NDC 68151-2014 Propranolol Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-2014 - Propranolol Hydrochloride
Product Characteristics
Product Packages
NDC Code 68151-2014-7
Package Description: 1 TABLET in 1 CUP
Product Details
What is NDC 68151-2014?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Propranolol Hydrochloride?
- RxCUI: 856457 - propranolol HCl 20 MG Oral Tablet
- RxCUI: 856457 - propranolol hydrochloride 20 MG Oral Tablet
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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".