Product Details for ANDA 074556
ACYCLOVIR (ACYCLOVIR)
400MG
Marketing Status: Prescription
800MG
Marketing Status: Prescription
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
400MG
Marketing Status: Prescription
Active Ingredient: ACYCLOVIR
Proprietary Name: ACYCLOVIR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A074556
Product Number: 002
Approval Date: Apr 22, 1997
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Prescription
Patent and Exclusivity Information
ACYCLOVIR (ACYCLOVIR)
Proprietary Name: ACYCLOVIR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A074556
Product Number: 002
Approval Date: Apr 22, 1997
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Prescription
Patent and Exclusivity Information
800MG
Marketing Status: Prescription
Active Ingredient: ACYCLOVIR
Proprietary Name: ACYCLOVIR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 800MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A074556
Product Number: 003
Approval Date: Apr 22, 1997
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Prescription
Patent and Exclusivity Information
ACYCLOVIR (ACYCLOVIR)
Proprietary Name: ACYCLOVIR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 800MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A074556
Product Number: 003
Approval Date: Apr 22, 1997
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Prescription
Patent and Exclusivity Information
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: ACYCLOVIR
Proprietary Name: ACYCLOVIR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074556
Product Number: 001
Approval Date: Apr 22, 1997
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: ACYCLOVIR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074556
Product Number: 001
Approval Date: Apr 22, 1997
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information