54569-0557 NDC - PROPRANOLOL HYDROCHLORIDE ()

Drug Information

Product NDC: 54569-0557

Proprietary Name: Propranolol Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: A-S Medication Solutions
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/21/2010

Package Information

No. Package Code Package Description Billing Unit
154569-0557-1100 TABLET in 1 BOTTLE (54569-0557-1)EA
254569-0557-260 TABLET in 1 BOTTLE (54569-0557-2)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC54569-0557The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEPropranolol HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/21/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEA-S Medication SolutionsName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023