Product Details for NDA 004041
DIETHYLSTILBESTROL (DIETHYLSTILBESTROL)
0.1MG
Marketing Status: Discontinued
0.5MG
Marketing Status: Discontinued
1MG
Marketing Status: Discontinued
5MG
Marketing Status: Discontinued
0.1MG
Marketing Status: Discontinued
Active Ingredient: DIETHYLSTILBESTROL
Proprietary Name: DIETHYLSTILBESTROL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N004041
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
DIETHYLSTILBESTROL (DIETHYLSTILBESTROL)
Proprietary Name: DIETHYLSTILBESTROL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N004041
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
0.5MG
Marketing Status: Discontinued
Active Ingredient: DIETHYLSTILBESTROL
Proprietary Name: DIETHYLSTILBESTROL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N004041
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
DIETHYLSTILBESTROL (DIETHYLSTILBESTROL)
Proprietary Name: DIETHYLSTILBESTROL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N004041
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
1MG
Marketing Status: Discontinued
Active Ingredient: DIETHYLSTILBESTROL
Proprietary Name: DIETHYLSTILBESTROL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N004041
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
DIETHYLSTILBESTROL (DIETHYLSTILBESTROL)
Proprietary Name: DIETHYLSTILBESTROL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N004041
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
5MG
Marketing Status: Discontinued
Active Ingredient: DIETHYLSTILBESTROL
Proprietary Name: DIETHYLSTILBESTROL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N004041
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: DIETHYLSTILBESTROL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N004041
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status: Discontinued
Patent and Exclusivity Information