Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 011283

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KENACORT (TRIAMCINOLONE)
1MG
Marketing Status: Discontinued

Active Ingredient: TRIAMCINOLONE
Proprietary Name: KENACORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N011283
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: DELCOR ASSET CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

KENACORT (TRIAMCINOLONE)
2MG
Marketing Status: Discontinued

Active Ingredient: TRIAMCINOLONE
Proprietary Name: KENACORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N011283
Product Number: 008
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: DELCOR ASSET CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

KENACORT (TRIAMCINOLONE)
4MG
Marketing Status: Discontinued

Active Ingredient: TRIAMCINOLONE
Proprietary Name: KENACORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 4MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N011283
Product Number: 006
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: DELCOR ASSET CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

KENACORT (TRIAMCINOLONE)
8MG
Marketing Status: Discontinued

Active Ingredient: TRIAMCINOLONE
Proprietary Name: KENACORT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 8MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N011283
Product Number: 010
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: DELCOR ASSET CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information