Product Details for NDA 019669
QUESTRAN LIGHT (CHOLESTYRAMINE)
EQ 4GM RESIN/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 4GM RESIN/SCOOPFUL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 4GM RESIN/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: CHOLESTYRAMINE
Proprietary Name: QUESTRAN LIGHT
Dosage Form; Route of Administration: POWDER; ORAL
Strength: EQ 4GM RESIN/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019669
Product Number: 001
Approval Date: Dec 5, 1988
Applicant Holder Full Name: BRISTOL MYERS CO
Marketing Status: Discontinued
Patent and Exclusivity Information
QUESTRAN LIGHT (CHOLESTYRAMINE)
Proprietary Name: QUESTRAN LIGHT
Dosage Form; Route of Administration: POWDER; ORAL
Strength: EQ 4GM RESIN/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019669
Product Number: 001
Approval Date: Dec 5, 1988
Applicant Holder Full Name: BRISTOL MYERS CO
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 4GM RESIN/SCOOPFUL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: CHOLESTYRAMINE
Proprietary Name: QUESTRAN LIGHT
Dosage Form; Route of Administration: POWDER; ORAL
Strength: EQ 4GM RESIN/SCOOPFUL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019669
Product Number: 003
Approval Date: Dec 5, 1988
Applicant Holder Full Name: BRISTOL MYERS CO
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: QUESTRAN LIGHT
Dosage Form; Route of Administration: POWDER; ORAL
Strength: EQ 4GM RESIN/SCOOPFUL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019669
Product Number: 003
Approval Date: Dec 5, 1988
Applicant Holder Full Name: BRISTOL MYERS CO
Marketing Status: Discontinued
Patent and Exclusivity Information