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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 086530

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SECONAL SODIUM (SECOBARBITAL SODIUM)
30MG
Marketing Status: Discontinued
Active Ingredient: SECOBARBITAL SODIUM
Proprietary Name: SECONAL SODIUM
Dosage Form; Route of Administration: SUPPOSITORY; RECTAL
Strength: 30MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A086530
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
SECONAL SODIUM (SECOBARBITAL SODIUM)
60MG
Marketing Status: Discontinued
Active Ingredient: SECOBARBITAL SODIUM
Proprietary Name: SECONAL SODIUM
Dosage Form; Route of Administration: SUPPOSITORY; RECTAL
Strength: 60MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A086530
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
SECONAL SODIUM (SECOBARBITAL SODIUM)
120MG
Marketing Status: Discontinued
Active Ingredient: SECOBARBITAL SODIUM
Proprietary Name: SECONAL SODIUM
Dosage Form; Route of Administration: SUPPOSITORY; RECTAL
Strength: 120MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A086530
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
SECONAL SODIUM (SECOBARBITAL SODIUM)
200MG
Marketing Status: Discontinued
Active Ingredient: SECOBARBITAL SODIUM
Proprietary Name: SECONAL SODIUM
Dosage Form; Route of Administration: SUPPOSITORY; RECTAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A086530
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
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