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Questran LightDrug - Questran Light The trade name of the product as shown on the labeling.
Dosage -
POWDER; ORAL
Active Ingredient(s) -
Cholestyramine
Strength -
EQ 4GM RESIN/PACKET
Applicant -
BRISTOL MYERS
New Drug Application (NDA) Number -
019669
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Dec 5, 1988
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Bristol Myers Co
Questran Light
Locholest Light Eq 4gm Resin/packet Powder; Oral
Locholest Light Eq 4gm Resin/scoopful Powder; Oral Prevalite Eq 4gm Resin/packet Powder; Oral Prevalite Eq 4gm Resin/scoopful Powder; Oral Questran Eq 4gm Resin/packet Powder; Oral Questran Eq 4gm Resin/scoopful Powder; Oral Questran Light Eq 4gm Resin/packet Powder; Oral Cholestyramine Light Eq 4gm Resin/scoopful Powder; Oral Locholest Eq 4gm Resin/packet Powder; Oral Locholest Eq 4gm Resin/scoopful Powder; Oral NewDrugInformation |