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FDA shortage status: Sufentanil Citrate Injection

FDA shortage status · Source checked 2026-10-06T18:55:41+00:00

FDA source answer

FDA currently lists this ingredient in shortage.

FDA source statuses: Current. First FDA posting: 2022-05-03. Latest FDA row update: 2026-09-22.

FDA lists 4 package records, with companies: Hikma Pharmaceuticals USA, Inc., Hospira, Inc., Hospira, Inc., a Pfizer Company. Package NDCs: 0409-3382-21, 17478-050-01, 17478-050-02, 17478-050-05.

FDA shortage reason: Other

This is nationwide FDA status, not local pharmacy inventory. CiteFacts does not provide medical, treatment, substitution, or dosing advice.

FDA package and manufacturer records

CompanyPackage NDCPresentationFDA availability fieldFDA update
Hikma Pharmaceuticals USA, Inc.17478-050-01Sufentanil Citrate, Injection, 50 mcg/1 mL (NDC 17478-050-01)Unavailable2026-09-18
Hikma Pharmaceuticals USA, Inc.17478-050-02Sufentanil Citrate, Injection, 50 mcg/1 mL (NDC 17478-050-02)Unavailable2026-09-18
Hikma Pharmaceuticals USA, Inc.17478-050-05Sufentanil Citrate, Injection, 50 mcg/1 mL (NDC 17478-050-05)Unavailable2026-09-18
Hospira, Inc., a Pfizer Company0409-3382-21Sufentanil Citrate, Injection, 50 ug/1 mL (NDC 0409-3382-21)Available2026-09-22

Source facts

Grouped generic ingredient: Sufentanil Citrate Injection · 4 package records

Therapeutic categories: Analgesia/Addiction, Pediatric
Dosage forms: Injection
Routes: EPIDURAL, INTRAVENOUS

Open FDA source data · JSON · Markdown

FDA is authoritative. Source retrieved 2026-10-06T18:55:41+00:00. Derived grouping is documented in this record's derivations.