Product Details for NDA 016273
LASIX (FUROSEMIDE)
20MG
Marketing Status: Prescription
40MG
Marketing Status: Prescription
80MG
Marketing Status: Prescription
20MG
Marketing Status: Prescription
Active Ingredient: FUROSEMIDE
Proprietary Name: LASIX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N016273
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: VALIDUS PHARMACEUTICALS LLC
Marketing Status: Prescription
Patent and Exclusivity Information
LASIX (FUROSEMIDE)
Proprietary Name: LASIX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N016273
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: VALIDUS PHARMACEUTICALS LLC
Marketing Status: Prescription
Patent and Exclusivity Information
40MG
Marketing Status: Prescription
Active Ingredient: FUROSEMIDE
Proprietary Name: LASIX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N016273
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: VALIDUS PHARMACEUTICALS LLC
Marketing Status: Prescription
Patent and Exclusivity Information
LASIX (FUROSEMIDE)
Proprietary Name: LASIX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N016273
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: VALIDUS PHARMACEUTICALS LLC
Marketing Status: Prescription
Patent and Exclusivity Information
80MG
Marketing Status: Prescription
Active Ingredient: FUROSEMIDE
Proprietary Name: LASIX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 80MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N016273
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: VALIDUS PHARMACEUTICALS LLC
Marketing Status: Prescription
Patent and Exclusivity Information
Proprietary Name: LASIX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 80MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N016273
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: VALIDUS PHARMACEUTICALS LLC
Marketing Status: Prescription
Patent and Exclusivity Information