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FDA Drug Approval, N017851, LIORESAL
FDA Drug Approval, N017851, LIORESAL
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NDA: 017851
Company: NOVARTIS
Drug Name: LIORESAL
Active Ingredients: BACLOFEN
Strength: 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: TABLET;ORAL
Action Date: 11/22/1977
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity
Company: NOVARTIS
Drug Name: LIORESAL
Active Ingredients: BACLOFEN
Strength: 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: TABLET;ORAL
Action Date: 11/22/1977
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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