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Data / Drug companies / Hospira, Inc.

Hospira, Inc.: 28 products in the FDA NDC directory, labeler code 61703

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Hospira, Inc. (labeler code 61703) lists 28 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 28 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on April 8, 2025.

The request: Watch Hospira, Inc. (FDA labeler code 61703): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
61703
Products in commercial distribution
28
Packages
40
Finished drugs by generic name
10
Prescription products
28
Over the counter products
0
Flagged as original packager
17 of 17 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
June 4, 1990
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)2278.6%
New drug applications (NDA)621.4%

Products by type

TypeProductsShare
Prescription drugs28100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Injection, solution2485.7%
Injection, solution, concentrate27.1%
Injection, powder, lyophilized, for solution27.1%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Paclitaxel61703-015Injection, solutionGeneric drugs (ANDA)April 8, 2025
Cytarabine61703-155Injection, solutionGeneric drugs (ANDA)April 7, 2025
Methotrexate61703-161Injection, solutionNew drug applications (NDA)November 4, 2024
Methotrexate61703-124Injection, solutionNew drug applications (NDA)October 17, 2022
Carboplatin61703-600Injection, solutionGeneric drugs (ANDA)May 23, 2022
Carboplatin61703-360Injection, solutionGeneric drugs (ANDA)May 23, 2022
Carboplatin61703-262Injection, solutionGeneric drugs (ANDA)May 23, 2022
Carboplatin61703-150Injection, solutionGeneric drugs (ANDA)May 23, 2022
Methotrexate61703-350Injection, solutionNew drug applications (NDA)September 25, 2014
VinCRIStine Sulfate61703-309Injection, solutionGeneric drugs (ANDA)November 27, 2013
Methotrexate61703-408Injection, solutionNew drug applications (NDA)November 11, 2013
Oxaliplatin61703-363Injection, solution, concentrateGeneric drugs (ANDA)August 10, 2009
Irinotecan Hydrochloride61703-349Injection, solutionGeneric drugs (ANDA)February 27, 2008
Mitoxantrone61703-343Injection, solution, concentrateGeneric drugs (ANDA)April 11, 2006
Pamidronate Disodium61703-326Injection, solutionGeneric drugs (ANDA)October 1, 2005
Pamidronate Disodium61703-324Injection, solutionGeneric drugs (ANDA)October 1, 2005
Methotrexate61703-350Injection, solutionNew drug applications (NDA)July 27, 2005
Carboplatin61703-339Injection, solutionGeneric drugs (ANDA)October 14, 2004
Paclitaxel61703-342Injection, solutionGeneric drugs (ANDA)March 1, 2004
Pamidronate Disodium61703-325Injection, solutionGeneric drugs (ANDA)July 28, 2003
Methotrexate61703-408Injection, solutionNew drug applications (NDA)February 26, 2001
Bleomycin61703-332Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 11, 2000
Bleomycin61703-323Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 10, 2000
Cytarabine61703-319Injection, solutionGeneric drugs (ANDA)November 22, 1999
VinCRIStine Sulfate61703-309Injection, solutionGeneric drugs (ANDA)January 1, 1996

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.