Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018569

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FUROSEMIDE (FUROSEMIDE)
20MG
Marketing Status: Prescription

Active Ingredient: FUROSEMIDE
Proprietary Name: FUROSEMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: N018569
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: EPIC PHARMA LLC
Marketing Status:  Prescription
Patent and Exclusivity Information

FUROSEMIDE (FUROSEMIDE)
40MG
Marketing Status: Prescription

Active Ingredient: FUROSEMIDE
Proprietary Name: FUROSEMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: N018569
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: EPIC PHARMA LLC
Marketing Status:  Prescription
Patent and Exclusivity Information

FUROSEMIDE (FUROSEMIDE)
80MG
Marketing Status: Prescription

Active Ingredient: FUROSEMIDE
Proprietary Name: FUROSEMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 80MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: N018569
Product Number: 005
Approval Date: Aug 14, 1984
Applicant Holder Full Name: EPIC PHARMA LLC
Marketing Status:  Prescription
Patent and Exclusivity Information