Active Ingredient: RAUWOLFIA SERPENTINA ROOT
Proprietary Name: RAUDIXIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N008842
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: RAUWOLFIA SERPENTINA ROOT
Proprietary Name: RAUDIXIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N008842
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status:
Discontinued
Patent and Exclusivity Information