Dextrose 50 mg per 1 mL injection, solution

Where it's made

This label doesn't name the factory that makes the drug. 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

• Nov 30, 2021 · Class II · Pfizer Inc.
  Lack of sterility assurance: bag has the potential to leak.
  Lots: Lot: 4923608 Exp. 1MAY2022
• Mar 5, 2015 · Class II · Hospira Inc.
  Lack of Assurance of Sterility: there is a potential for solution to leak at the administrative port of the primary container.
  Lots: Lot: 37-042-JT, Exp 1JAN2016

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

Product details

Generic drug

Anhydrous Dextrose: every company that makes it

Form

injection, solution, intravenous

Strength

50 mg per 1 mL

Approval

NDA NDA019466

On the market since

Jun 27, 2005

Package NDCs

0409-7100-02 0409-7100-04 0409-7100-66 0409-7100-67 0409-7100-68 0409-7100-69

Official label

DailyMed (National Library of Medicine), updated Jun 2, 2026

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