Product Details for ANDA 078101
LEVETIRACETAM (LEVETIRACETAM)
250MG
Marketing Status: Discontinued
500MG
Marketing Status: Discontinued
750MG
Marketing Status: Discontinued
1GM
Marketing Status: Discontinued
250MG
Marketing Status: Discontinued
Active Ingredient: LEVETIRACETAM
Proprietary Name: LEVETIRACETAM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078101
Product Number: 001
Approval Date: Jan 15, 2009
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status: Discontinued
Patent and Exclusivity Information
LEVETIRACETAM (LEVETIRACETAM)
Proprietary Name: LEVETIRACETAM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078101
Product Number: 001
Approval Date: Jan 15, 2009
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status: Discontinued
Patent and Exclusivity Information
500MG
Marketing Status: Discontinued
Active Ingredient: LEVETIRACETAM
Proprietary Name: LEVETIRACETAM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078101
Product Number: 002
Approval Date: Jan 15, 2009
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status: Discontinued
Patent and Exclusivity Information
LEVETIRACETAM (LEVETIRACETAM)
Proprietary Name: LEVETIRACETAM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078101
Product Number: 002
Approval Date: Jan 15, 2009
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status: Discontinued
Patent and Exclusivity Information
750MG
Marketing Status: Discontinued
Active Ingredient: LEVETIRACETAM
Proprietary Name: LEVETIRACETAM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 750MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078101
Product Number: 003
Approval Date: Jan 15, 2009
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status: Discontinued
Patent and Exclusivity Information
LEVETIRACETAM (LEVETIRACETAM)
Proprietary Name: LEVETIRACETAM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 750MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078101
Product Number: 003
Approval Date: Jan 15, 2009
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status: Discontinued
Patent and Exclusivity Information
1GM
Marketing Status: Discontinued
Active Ingredient: LEVETIRACETAM
Proprietary Name: LEVETIRACETAM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1GM
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078101
Product Number: 004
Approval Date: Jan 15, 2009
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: LEVETIRACETAM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1GM
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078101
Product Number: 004
Approval Date: Jan 15, 2009
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status: Discontinued
Patent and Exclusivity Information