61703-363 NDC - OXALIPLATIN ()

Drug Information

  • Product NDC: 61703-363
  • Proprietary Name: Oxaliplatin
  • Non Proprietary Name:
  • Active Ingredient(s): 5 mg/mL OXALIPLATIN
  • Administration Route(s):
  • Dosage Form(s):
  • Pharmacy Class(es): Platinum-based Drug [EPC]; Platinum-containing Compounds [EXT]

Labeler Information

Field Name Field Value
Labeler Name: Hospira Worldwide, Inc.
Product Type:
FDA Application Number: ANDA078813
Marketing Category: ANDA
Start Marketing Date:8/25/2009
End Marketing Date:5/20/2015

Package Information

No. Package Code Package Description Billing Unit
161703-363-181 VIAL, SINGLE-DOSE in 1 CARTON (61703-363-18) / 10 mL in 1 VIAL, SINGLE-DOSEML
261703-363-181 VIAL, SINGLE-USE in 1 CARTON (61703-363-18) / 10 mL in 1 VIAL, SINGLE-USEML
361703-363-221 VIAL, SINGLE-DOSE in 1 CARTON (61703-363-22) / 20 mL in 1 VIAL, SINGLE-DOSEML
461703-363-221 VIAL, SINGLE-USE in 1 CARTON (61703-363-22) / 20 mL in 1 VIAL, SINGLE-USEML

NDC Record

Field Name Field Value Definition
PRODUCT NDC61703-363The 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 NAMEOxaliplatinThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/25/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERANDA078813This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEHospira Worldwide, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC61703-363The 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 NAMEOxaliplatinThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/10/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERANDA078813This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEHospira, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 8/8/2025

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