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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 017618

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BRICANYL (TERBUTALINE SULFATE)
2.5MG
Marketing Status: Discontinued
Active Ingredient: TERBUTALINE SULFATE
Proprietary Name: BRICANYL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N017618
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information
BRICANYL (TERBUTALINE SULFATE)
5MG
Marketing Status: Discontinued
Active Ingredient: TERBUTALINE SULFATE
Proprietary Name: BRICANYL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N017618
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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