U.S. flag An official website of the United States government
  1. Home
  2. Drug Databases
  3. Orange Book Home

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 019500

Expand all

LAMPRENE (CLOFAZIMINE)
50MG
Marketing Status: Discontinued
Active Ingredient: CLOFAZIMINE
Proprietary Name: LAMPRENE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 50MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N019500
Product Number: 002
Approval Date: Dec 15, 1986
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information
LAMPRENE (CLOFAZIMINE)
100MG
Marketing Status: Discontinued
Active Ingredient: CLOFAZIMINE
Proprietary Name: LAMPRENE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019500
Product Number: 001
Approval Date: Dec 15, 1986
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information
Back to Top