Heparin Sodium and Dextrose 10000 [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

• Jun 6, 2014 · Class II · Hospira Inc.
  Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking from primary container of bag.
  Lots: Lot # 34-811-KL, 36-106-KL, 36-114-KL; Exp. 12/15; 36-101-KL, Exp. 12/15; 37-202-KL, Exp. 1/16; 38-302-KL, Exp. 2/16; 38-305-KL, Exp. 2/16

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

10000 [USP'U] per 100 mL

Approval

NDA NDA019339

On the market since

Dec 12, 2022

Package NDCs

0409-4520-02 0409-4520-30

Official label

DailyMed (National Library of Medicine), updated May 25, 2026

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