Product Details for ANDA 040321
METHYLPHENIDATE HYDROCHLORIDE (METHYLPHENIDATE HYDROCHLORIDE)
5MG
Marketing Status: Discontinued
10MG
Marketing Status: Discontinued
20MG
Marketing Status: Discontinued
5MG
Marketing Status: Discontinued
Active Ingredient: METHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040321
Product Number: 001
Approval Date: Feb 5, 2002
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
METHYLPHENIDATE HYDROCHLORIDE (METHYLPHENIDATE HYDROCHLORIDE)
Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040321
Product Number: 001
Approval Date: Feb 5, 2002
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
10MG
Marketing Status: Discontinued
Active Ingredient: METHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040321
Product Number: 002
Approval Date: Feb 5, 2002
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
METHYLPHENIDATE HYDROCHLORIDE (METHYLPHENIDATE HYDROCHLORIDE)
Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040321
Product Number: 002
Approval Date: Feb 5, 2002
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
20MG
Marketing Status: Discontinued
Active Ingredient: METHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040321
Product Number: 003
Approval Date: Feb 5, 2002
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040321
Product Number: 003
Approval Date: Feb 5, 2002
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information