57277-001 NDC - OXALIPLATIN ()

Drug Information

Product NDC: 57277-001

Proprietary Name: Oxaliplatin

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Sanja Pharmaceuticals Company
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	9/21/2017

No.	Package Code	Package Description	Billing Unit
1	57277-001-05	1 VIAL in 1 CARTON (57277-001-05) / 10 mL in 1 VIAL

Field Name	Field Value	Definition
PRODUCT NDC	57277-001	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	Oxaliplatin	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	9/21/2017	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Sanja Pharmaceuticals Company	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