Active Ingredient: HYDROMORPHONE HYDROCHLORIDE
Proprietary Name: HYDROMORPHONE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 5MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A074653
Product Number: 001
Approval Date: Jul 29, 1998
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
