55648-185 NDC - ZOLEDRONIC ACID ()

Drug Information

Product NDC: 55648-185

Proprietary Name: Zoledronic Acid

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Wockhardt Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/2/2013

Package Information

No. Package Code Package Description Billing Unit
155648-185-011 BOTTLE in 1 CARTON (55648-185-01) > 100 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC55648-185The 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 NAMEZoledronic AcidThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/2/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWockhardt LimitedName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/18/2019