DEA Schedule CII
Strength
10 mg/1
Manufacturer
Amneal Pharmaceuticals of New York LLCNDC
00115123201
Classification
Generic
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Last Updated
5/19/2021
Active Ingredients
OXYMORPHONE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA079087On Market Since
1/2/2013
Pharmacological Classes
Full Opioid Agonists
Opioid Agonist
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