Product Details for NDA 007794
NEOTHYLLINE (DYPHYLLINE)
160MG/15ML
Marketing Status: Discontinued
200MG
Marketing Status: Discontinued
400MG
Marketing Status: Discontinued
160MG/15ML
Marketing Status: Discontinued
Active Ingredient: DYPHYLLINE
Proprietary Name: NEOTHYLLINE
Dosage Form; Route of Administration: ELIXIR; ORAL
Strength: 160MG/15ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N007794
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
NEOTHYLLINE (DYPHYLLINE)
Proprietary Name: NEOTHYLLINE
Dosage Form; Route of Administration: ELIXIR; ORAL
Strength: 160MG/15ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N007794
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
200MG
Marketing Status: Discontinued
Active Ingredient: DYPHYLLINE
Proprietary Name: NEOTHYLLINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N007794
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
NEOTHYLLINE (DYPHYLLINE)
Proprietary Name: NEOTHYLLINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N007794
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
400MG
Marketing Status: Discontinued
Active Ingredient: DYPHYLLINE
Proprietary Name: NEOTHYLLINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N007794
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: NEOTHYLLINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N007794
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information