Product Details for ANDA 077471
HYDROMORPHONE HYDROCHLORIDE (HYDROMORPHONE HYDROCHLORIDE)
2MG
Marketing Status: Discontinued
4MG
Marketing Status: Discontinued
8MG
Marketing Status: Discontinued
2MG
Marketing Status: Discontinued
Active Ingredient: HYDROMORPHONE HYDROCHLORIDE
Proprietary Name: HYDROMORPHONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077471
Product Number: 002
Approval Date: Dec 9, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
HYDROMORPHONE HYDROCHLORIDE (HYDROMORPHONE HYDROCHLORIDE)
Proprietary Name: HYDROMORPHONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077471
Product Number: 002
Approval Date: Dec 9, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
4MG
Marketing Status: Discontinued
Active Ingredient: HYDROMORPHONE HYDROCHLORIDE
Proprietary Name: HYDROMORPHONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 4MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077471
Product Number: 003
Approval Date: Dec 9, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
HYDROMORPHONE HYDROCHLORIDE (HYDROMORPHONE HYDROCHLORIDE)
Proprietary Name: HYDROMORPHONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 4MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077471
Product Number: 003
Approval Date: Dec 9, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
8MG
Marketing Status: Discontinued
Active Ingredient: HYDROMORPHONE HYDROCHLORIDE
Proprietary Name: HYDROMORPHONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 8MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077471
Product Number: 001
Approval Date: Dec 9, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: HYDROMORPHONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 8MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077471
Product Number: 001
Approval Date: Dec 9, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information