Product Details for ANDA 076193
PROPAFENONE HYDROCHLORIDE (PROPAFENONE HYDROCHLORIDE)
150MG
Marketing Status: Discontinued
225MG
Marketing Status: Discontinued
300MG
Marketing Status: Discontinued
150MG
Marketing Status: Discontinued
Active Ingredient: PROPAFENONE HYDROCHLORIDE
Proprietary Name: PROPAFENONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076193
Product Number: 001
Approval Date: Feb 7, 2002
Applicant Holder Full Name: NESHER PHARMACEUTICALS USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
PROPAFENONE HYDROCHLORIDE (PROPAFENONE HYDROCHLORIDE)
Proprietary Name: PROPAFENONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076193
Product Number: 001
Approval Date: Feb 7, 2002
Applicant Holder Full Name: NESHER PHARMACEUTICALS USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
225MG
Marketing Status: Discontinued
Active Ingredient: PROPAFENONE HYDROCHLORIDE
Proprietary Name: PROPAFENONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 225MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076193
Product Number: 002
Approval Date: Feb 7, 2002
Applicant Holder Full Name: NESHER PHARMACEUTICALS USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
PROPAFENONE HYDROCHLORIDE (PROPAFENONE HYDROCHLORIDE)
Proprietary Name: PROPAFENONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 225MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076193
Product Number: 002
Approval Date: Feb 7, 2002
Applicant Holder Full Name: NESHER PHARMACEUTICALS USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
300MG
Marketing Status: Discontinued
Active Ingredient: PROPAFENONE HYDROCHLORIDE
Proprietary Name: PROPAFENONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076193
Product Number: 003
Approval Date: Feb 7, 2002
Applicant Holder Full Name: NESHER PHARMACEUTICALS USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: PROPAFENONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076193
Product Number: 003
Approval Date: Feb 7, 2002
Applicant Holder Full Name: NESHER PHARMACEUTICALS USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information