NDC 51662-1702

Ketorolac Tromethamine 30 mg per 1 mL injection, solution

On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Fresenius Kabi, LLC's NDC 63323-162.

Where the pills inside were made

Factory	Where	Role	Last FDA inspection
Fresenius Kabi USA, LLC	Grand Island, NY, United States	Makes it and tests it	Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action
Fresenius Kabi USA, LLC	Melrose Park, IL, United States	Makes it and tests it	Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action

Dec 23, 2020 · Class I · Fresenius Kabi USA, LLC
Presence of Particulate Matter - found in reserve sample vials at the firm.
Lots: Lot # 6121083, Exp 2/2021
Dec 17, 2020 · Class II · Fresenius Kabi USA, LLC
Presence of Particulate Matter - found in reserve sample vials at the firm.
Lots: Batch # 6121125, Exp 02/2021
Apr 20, 2020 · Class I · Fresenius Kabi USA, LLC
Presence of Particulate Matter - found in reserve sample vials at the firm.
Lots: Lot #: 6118737, 6118902, Exp 04/2020; 6119052, Exp 05/2020; 6119752, Exp 08/2020; 6122349, Exp 07/2021; 6122538, Exp 09/2021
Apr 20, 2020 · Class II · Fresenius Kabi USA, LLC
Presence of Particulate Matter - found in reserve sample vials at the firm.
Lots: Lot #: 6119229, 6119273, Exp 06/2020; 6119843, Exp 09/2020; 6121115, Exp 02/2021; 6121451, 6121452, 6121496, Exp 03/2021

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

Generic drug: Ketorolac: every company that makes it
Form: injection, solution, intramuscular
Strength: 30 mg per 1 mL
Approval: ANDA ANDA075784
On the market since: Oct 18, 2000
Package NDCs: 51662-1702-1 51662-1702-2 51662-1702-3
Official label: DailyMed (National Library of Medicine), updated Aug 18, 2026

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