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US ATC N02AA03 · updated 2 Nov 2026

Hydromorphone shortage in United States

Is there a Hydromorphone shortage in United States?

Yes. As of 2 Nov 2026, 27 Hydromorphone products are reported short in United States, the first since 31 Oct 2017. No return date has been given. Main reason: not stated.

Also short in Canada, Germany, Switzerland, Sweden. All countries.

Affected products in United States

CountryProductCompanySinceExpected backReason
USDilaudid, Injection, 1 mg/1 mL (NDC 76045-009-06)Fresenius Kabi USA, LLC31 Oct 2017not givenOther
USDilaudid, Injection, 1 mg/1 mL (NDC 76045-009-11)Fresenius Kabi USA, LLC31 Oct 2017not givenOther
USHydromorphone Hydrochloride, Injection, 1 mg/1 mL (NDC 0409-1283-37)Hospira, Inc., a Pfizer Company31 Oct 2017not givenOther
USHydromorphone Hydrochloride, Injection, 1 mg/1 mL (NDC 63323-852-25)Fresenius Kabi USA, LLC31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 1 mg/1 mL Syringes (NDC 0409-1283-31)Hospira, Inc., a Pfizer Company31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 10 mg/1 mL (NDC 0409-2634-01)Hospira, Inc., a Pfizer Company31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 10 mg/1 mL (NDC 63323-851-10)Fresenius Kabi USA, LLC31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 10 mg/1 mL (NDC 63323-851-15)Fresenius Kabi USA, LLC31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 10 mg/1 mL (NDC 63323-851-50)Fresenius Kabi USA, LLC31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 2 mg/1 mL (NDC 0409-1312-36) limitedHospira, Inc., a Pfizer Company31 Oct 2017not givenOther
USHydromorphone Hydrochloride, Injection, 2 mg/1 mL (NDC 0409-3365-10)Hospira, Inc., a Pfizer Company31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 2 mg/1 mL (NDC 63323-853-25)Fresenius Kabi USA, LLC31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 2 mg/1 mL Syringes (NDC 0409-1312-30)Hospira, Inc., a Pfizer Company31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 4 mg/1 mL Syringes (NDC 0409-1304-31)Hospira, Inc., a Pfizer Company31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 50 mg/5 mL (10 mg/mL) (NDC 0409-2634-05)Hospira, Inc., a Pfizer Company31 Oct 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 500 mg/50 mL (10 mg/mL) (NDC 0409-2634-50)Hospira, Inc., a Pfizer Company31 Oct 2017not givenNot stated
USDilaudid, Injection, .2 mg/1 mL (NDC 76045-121-11)Fresenius Kabi USA, LLC1 Nov 2017not givenOther
USDilaudid, Injection, 2 mg/1 mL (NDC 76045-010-11)Fresenius Kabi USA, LLC1 Nov 2017not givenOther
USHydromorphone Hydrochloride, Injection, 0.25 mg/ 0.5 mL NexJect™ Single-dose Syringe Luer Lock (no needle) (NDC 0409-1805-01)Hospira, Inc., a Pfizer Company1 Nov 2017not givenOther
USHydromorphone Hydrochloride, Injection, 0.5 mg/0.5 mL NexJect™ Single-dose Syringe Luer Lock (no needle) (NDC 0409-4264-01) limitedHospira, Inc., a Pfizer Company1 Nov 2017not givenOther
USHydromorphone Hydrochloride, Injection, 10 mg/1 mL (NDC 0703-0018-01)Teva Pharmaceuticals USA, Inc.1 Nov 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 10 mg/1 mL (NDC 0703-0110-03)Teva Pharmaceuticals USA, Inc.1 Nov 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 10 mg/1 mL (NDC 0703-0113-03) limitedTeva Pharmaceuticals USA, Inc.1 Nov 2017not givenOther
USHydromorphone Hydrochloride, Injection, 2 mg/1 mL (NDC 0641-6254-01)Hikma Pharmaceuticals USA, Inc.1 Nov 2017not givenIncreased demand
Demand increase for the drug
USHydromorphone Hydrochloride, Injection, 4 mg/1 mL (NDC 63323-854-10)Fresenius Kabi USA, LLC1 Nov 2017not givenNot stated
USHydromorphone Hydrochloride, Injection, 2 mg/1 mL (NDC 0641-0121-25)Hikma Pharmaceuticals USA, Inc.3 Nov 2017not givenNot stated
USHydromorphone Hydrochloride, Suppository, 3 mg (NDC 0574-7224-06) discontinuationPadagis US LLC23 Jul 2026not givenNot stated

Source

U.S. Food and Drug Administration (FDA), Drug Shortages via openFDA. Official list. Shortages the FDA lists as current, plus products to be discontinued; one row per package (NDC).