45932-0029 NDC - VANCOMYCIN HYDROCHLORIDE ()

Drug Information

Product NDC: 45932-0029

Proprietary Name: Vancomycin Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Xellia Pharmaceuticals, ApS
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/10/2014

Package Information

No. Package Code Package Description Billing Unit
145932-0029-11 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (45932-0029-1)
245932-0029-210 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (45932-0029-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC45932-0029The 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 NAMEVancomycin 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 DATE4/10/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEXellia Pharmaceuticals, ApSName 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