NDC 23155-193

Colistimethate Sodium 150 mg per 4 mL injection, powder, lyophilized, for 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 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. names for other drugs.

Feb 25, 2015 · Class II · Heritage Pharmaceuticals, Inc.
Lack of Assurance of Sterility: Firm is recalling two injectable products due to concerns with quality control processes.
Lots: Lot # VCOA002; Exp. 09/14, VCOA003; Exp. 10/14, VCOA004; Exp. 10/14 VCOA005; Exp. 01/15, VCOA006; Exp 03/15, VCOA007; Exp 09/15, VCOA008; Exp. 12/15, VCOA009; Exp. 02/16, VCOA010; Exp. 10/16 VCOA011; Exp. 10/16

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

Generic drug: Colistimethate: every company that makes it
Form: injection, powder, lyophilized, for solution, intramuscular; intravenous
Strength: 150 mg per 4 mL
Approval: ANDA ANDA202359
On the market since: Sep 9, 2021
Package NDCs: 23155-193-31 23155-193-41
Official label: DailyMed (National Library of Medicine), updated Nov 4, 2026

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