DEA Schedule CII
Strength
2 mg/mL
Manufacturer
Fresenius Kabi USA, LLCNDC
63323085325
Classification
Generic
Dosage Form
INJECTION, SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Last Updated
4/22/2026
Active Ingredients
HYDROMORPHONE HYDROCHLORIDEApproval Type
New Drug (NDA)
FDA Application
NDA019034On Market Since
12/15/2017
Pharmacological Classes
Full Opioid Agonists
Opioid Agonist
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