54868-4576 NDC - BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE ()

Drug Information

Product NDC: 54868-4576

Proprietary Name: Bisoprolol Fumarate and Hydrochlorothiazide

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	54868-4576-0	30 TABLET, COATED in 1 BOTTLE (54868-4576-0)	EA
2	54868-4576-1	100 TABLET, COATED in 1 BOTTLE (54868-4576-1)	EA
3	54868-4576-2	60 TABLET, COATED in 1 BOTTLE (54868-4576-2)	EA
4	54868-4576-3	90 TABLET, COATED in 1 BOTTLE (54868-4576-3)	EA

Field Name	Field Value	Definition
PRODUCT NDC	54868-4576	The 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 NAME	Bisoprolol Fumarate and Hydrochlorothiazide	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	1/15/2002	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Physicians Total Care, Inc.	Name 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