Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 007600

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SURITAL (THIAMYLAL SODIUM)
1GM/VIAL
Marketing Status: Discontinued

Active Ingredient: THIAMYLAL SODIUM
Proprietary Name: SURITAL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1GM/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N007600
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKEDALE PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

SURITAL (THIAMYLAL SODIUM)
5GM/VIAL
Marketing Status: Discontinued

Active Ingredient: THIAMYLAL SODIUM
Proprietary Name: SURITAL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N007600
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKEDALE PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

SURITAL (THIAMYLAL SODIUM)
10GM/VIAL
Marketing Status: Discontinued

Active Ingredient: THIAMYLAL SODIUM
Proprietary Name: SURITAL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10GM/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N007600
Product Number: 009
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKEDALE PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information