Heparin Sodium 200 [USP'U] per 100 mL injection, solution

Where it's made

This label doesn't name the factory that makes the drug (it lists 1 site that tests it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Hospira, Inc. names for other drugs.

Recalls

• Dec 29, 2022 · Class II · Pfizer Inc.
  Lack of assurance of sterility: Bags have the potential to leak.
  Lots: Lot: 5935283, Exp. 12/01/2023
• Sep 11, 2014 · Class I · Hospira Inc.
  Presence of Particulate Matter: A particulate, confirmed as human hair, was found sealed between the tube and film at the round seal of the unused administrative port of the container.
  Lots: Lot #: 41-046-JT, Exp 11/01/2015
• Jan 9, 2014 · Class II · Hospira Inc.
  Lack of Assurance of Sterility; potential leakage from administrative port.
  Lots: Lot #: 26-125-JT, Exp: 8/14

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Heparin: every company that makes it

Form

injection, solution, intravenous

Strength

200 [USP'U] per 100 mL

Approval

NDA NDA018916

On the market since

Feb 27, 2023

Package NDCs

0409-1005-01 0409-1005-20

Official label

DailyMed (National Library of Medicine), updated May 12, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?