Product Details for NDA 011161
ARISTOCORT (TRIAMCINOLONE)
1MG
Marketing Status: Discontinued
2MG
Marketing Status: Discontinued
4MG
Marketing Status: Discontinued
8MG
Marketing Status: Discontinued
16MG
Marketing Status: Discontinued
1MG
Marketing Status: Discontinued
Active Ingredient: TRIAMCINOLONE
Proprietary Name: ARISTOCORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011161
Product Number: 009
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ASTELLAS PHARMA US INC
Marketing Status: Discontinued
Patent and Exclusivity Information
ARISTOCORT (TRIAMCINOLONE)
Proprietary Name: ARISTOCORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011161
Product Number: 009
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ASTELLAS PHARMA US INC
Marketing Status: Discontinued
Patent and Exclusivity Information
2MG
Marketing Status: Discontinued
Active Ingredient: TRIAMCINOLONE
Proprietary Name: ARISTOCORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011161
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ASTELLAS PHARMA US INC
Marketing Status: Discontinued
Patent and Exclusivity Information
ARISTOCORT (TRIAMCINOLONE)
Proprietary Name: ARISTOCORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011161
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ASTELLAS PHARMA US INC
Marketing Status: Discontinued
Patent and Exclusivity Information
4MG
Marketing Status: Discontinued
Active Ingredient: TRIAMCINOLONE
Proprietary Name: ARISTOCORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 4MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011161
Product Number: 007
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ASTELLAS PHARMA US INC
Marketing Status: Discontinued
Patent and Exclusivity Information
ARISTOCORT (TRIAMCINOLONE)
Proprietary Name: ARISTOCORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 4MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011161
Product Number: 007
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ASTELLAS PHARMA US INC
Marketing Status: Discontinued
Patent and Exclusivity Information
8MG
Marketing Status: Discontinued
Active Ingredient: TRIAMCINOLONE
Proprietary Name: ARISTOCORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 8MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011161
Product Number: 011
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ASTELLAS PHARMA US INC
Marketing Status: Discontinued
Patent and Exclusivity Information
ARISTOCORT (TRIAMCINOLONE)
Proprietary Name: ARISTOCORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 8MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011161
Product Number: 011
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ASTELLAS PHARMA US INC
Marketing Status: Discontinued
Patent and Exclusivity Information
16MG
Marketing Status: Discontinued
Active Ingredient: TRIAMCINOLONE
Proprietary Name: ARISTOCORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 16MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011161
Product Number: 010
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ASTELLAS PHARMA US INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: ARISTOCORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 16MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011161
Product Number: 010
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ASTELLAS PHARMA US INC
Marketing Status: Discontinued
Patent and Exclusivity Information