Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 017543

Expand all

LUDIOMIL (MAPROTILINE HYDROCHLORIDE)
25MG
Marketing Status: Discontinued

Active Ingredient: MAPROTILINE HYDROCHLORIDE
Proprietary Name: LUDIOMIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N017543
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

LUDIOMIL (MAPROTILINE HYDROCHLORIDE)
50MG
Marketing Status: Discontinued

Active Ingredient: MAPROTILINE HYDROCHLORIDE
Proprietary Name: LUDIOMIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N017543
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

LUDIOMIL (MAPROTILINE HYDROCHLORIDE)
75MG
Marketing Status: Discontinued

Active Ingredient: MAPROTILINE HYDROCHLORIDE
Proprietary Name: LUDIOMIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N017543
Product Number: 003
Approval Date: Sep 30, 1982
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information