43489-100 NDC - AMLODIPINE BESYLATE ()

Drug Information

Product NDC: 43489-100

Proprietary Name: Amlodipine Besylate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: China Resources Saike Pharmaceutical Co., Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/15/2011

Package Information

No. Package Code Package Description Billing Unit
143489-100-0190 TABLET in 1 BOTTLE, PLASTIC (43489-100-01)
243489-100-03500 TABLET in 1 BOTTLE, PLASTIC (43489-100-03)
343489-100-051000 TABLET in 1 BOTTLE, PLASTIC (43489-100-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43489-100The 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 NAMEAmlodipine BesylateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/15/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEChina Resources Saike Pharmaceutical Co., Ltd.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