Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 011521

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RAUWOLFIA SERPENTINA (RAUWOLFIA SERPENTINA ROOT)
50MG
Marketing Status: Discontinued

Active Ingredient: RAUWOLFIA SERPENTINA ROOT
Proprietary Name: RAUWOLFIA SERPENTINA
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N011521
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:  Discontinued
Patent and Exclusivity Information

RAUWOLFIA SERPENTINA (RAUWOLFIA SERPENTINA ROOT)
100MG
Marketing Status: Discontinued

Active Ingredient: RAUWOLFIA SERPENTINA ROOT
Proprietary Name: RAUWOLFIA SERPENTINA
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N011521
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:  Discontinued
Patent and Exclusivity Information