Active Ingredient: ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCODONE AND ACETAMINOPHEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG;7.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040789
Product Number: 001
Approval Date: Nov 27, 2007
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS NY LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCODONE AND ACETAMINOPHEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 650MG;10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040789
Product Number: 002
Approval Date: Nov 27, 2007
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS NY LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information