64679-739 NDC - AMIODARONE HYDROCHLORIDE ()

Drug Information

Product NDC: 64679-739

Proprietary Name: Amiodarone Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Wockhardt USA LLC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/30/2008

Package Information

No. Package Code Package Description Billing Unit
164679-739-011 VIAL in 1 CARTON (64679-739-01) / 3 mL in 1 VIAL
264679-739-0210 VIAL in 1 CARTON (64679-739-02) / 3 mL in 1 VIAL
364679-739-045 VIAL in 1 CARTON (64679-739-04) / 3 mL in 1 VIAL

NDC Record

Field Name Field Value Definition
PRODUCT NDC64679-739The 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 NAMEAmiodarone 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 DATE10/30/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWockhardt USA LLC.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