Due for re-check: the scheduled review date of 2026-09-11 has passed. Every value below still carries the source it was taken from and the passage that states it — check it against the link.
72572-127-10 · Dexmedetomidine Hydrochloride Injection · Azurity Pharmaceuticals, Inc
What is the package ndc for 72572-127-10 · Dexmedetomidine Hydrochloride Injection · Azurity Pharmaceuticals, Inc?
For 72572-127-10 · Dexmedetomidine Hydrochloride Injection · Azurity Pharmaceuticals, Inc, package ndc is 72572-127-10; generic name is Dexmedetomidine Hydrochloride Injection; manufacturer is Azurity Pharmaceuticals, Inc; status is Current; availability now is Available, recorded from its source on 2026-09-01; source re-checked 2026-09-08.
"initial_posting_date": "04/10/2020", "package_ndc": "72572-127-10", "generic_name": "Dexmedetomidine Hydrochloride Injection", "contact_info": "877-495-6856", "availability": "Available", "related_info": "Distributed by Civica"
— api.fda.gov, retrieved 2026-09-01
- Package NDC
- 72572-127-10 verified
- Generic name
- Dexmedetomidine Hydrochloride Injection verified
- Manufacturer
- Azurity Pharmaceuticals, Inc verified
- Status
- Current verified
- Availability now
- Available verified
- FDA note
- Distributed by Civica verified
- Initial posting date
- 04/10/2020 verified
- Last update date
- 08/17/2026 verified
- Days in shortage
- 2335 our reading
- Dosage form
- Injection verified
- Therapeutic category
- Anesthesia verified
Values marked our reading are our classification of what the source says — the source does not print them in those words. The quote below is the evidence for each one; judge it yourself.
Where each value comes from
The values above are stated away from the sentence quoted with the answer, so the passage that states them is shown here too.
Manufacturer, Status, Last update date, Dosage form and Therapeutic category
"update_date": "08/17/2026", "therapeutic_category": [ "Anesthesia" ], "dosage_form": "Injection", "presentation": "Dexmedetomidine Hydrochloride, Injection, 200 mcg/50 mL (4 ug/1 mL) (NDC 72572-127-10)", "company_name": "Azurity Pharmaceuticals, Inc", "status": "Current"
— all from api.fda.gov, retrieved 2026-09-01
Source
- api.fda.govhttps://api.fda.gov/drug/shortages.json?search=company_name%3A%22Azurity%20Pharmaceuticals,%20Inc%22+AND+generic_name%3A%22Dexmedetomidine%20Hydrochloride%20Injection%22+AND+status%3A%22Current%22&limit=1000