Active Ingredient: OXYMORPHONE HYDROCHLORIDE
Proprietary Name: OXYMORPHONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A202321
Product Number: 002
Approval Date: Apr 25, 2013
Applicant Holder Full Name: SPECGX LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information