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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 009268

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CHOLEDYL (OXTRIPHYLLINE)
100MG/5ML
Marketing Status: Discontinued
Active Ingredient: OXTRIPHYLLINE
Proprietary Name: CHOLEDYL
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 100MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N009268
Product Number: 012
Approval Date: Nov 27, 1984
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
CHOLEDYL (OXTRIPHYLLINE)
50MG/5ML
Marketing Status: Discontinued
Active Ingredient: OXTRIPHYLLINE
Proprietary Name: CHOLEDYL
Dosage Form; Route of Administration: SYRUP; ORAL
Strength: 50MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N009268
Product Number: 011
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
CHOLEDYL (OXTRIPHYLLINE)
100MG
Marketing Status: Discontinued
Active Ingredient: OXTRIPHYLLINE
Proprietary Name: CHOLEDYL
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N009268
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
CHOLEDYL (OXTRIPHYLLINE)
200MG
Marketing Status: Discontinued
Active Ingredient: OXTRIPHYLLINE
Proprietary Name: CHOLEDYL
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N009268
Product Number: 007
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
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