53808-1120 NDC - OLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE ()

Drug Information

Product NDC: 53808-1120

Proprietary Name: Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	53808-1120-1	30 TABLET, FILM COATED in 1 BLISTER PACK (53808-1120-1)

Field Name	Field Value	Definition
PRODUCT NDC	53808-1120	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	Olmesartan Medoxomil, Amlodipine 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	10/25/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	DOH CENTRAL PHARMACY	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024