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SotradecolDrug - Sotradecol The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
Active Ingredient(s) -
Sodium Tetradecyl Sulfate
Strength -
3% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Applicant -
ELKINS SINN
New Drug Application (NDA) Number -
005970
Product Number -
005
Therapeutic Equivalence (TE) Code -
Approval Date -
Approved Prior to Jan 1, 1982
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Elkins Sinn Div Ah Robins Co Inc
Sotradecol
Sodium Polystyrene Sulfonate 15gm/60ml Suspension; Oral, Rectal
Sodium Polystyrene Sulfonate 15gm/60ml Suspension; Oral, Rectal Sps 15gm/60ml Suspension; Oral, Rectal Sodium Succinate 30% Injectable; Injection Sotradecol 20mg/2ml (10mg/ml) Injectable; Injection Sotradecol 60mg/2ml (30mg/ml) Injectable; Injection Sotradecol 1% **federal Register Determination That Product Was Not Discontinued Or Withdrawn For Safety Or Efficacy Reasons** Injectable; Injection Sotradecol 3% **federal Register Determination That Product Was Not Discontinued Or Withdrawn For Safety Or Efficacy Reasons** Injectable; Injection Sodium Polystyrene Sulfonate 453.6gm/bot Powder; Oral, Rectal Sodium Polystyrene Sulfonate 15gm/60ml Suspension; Oral, Rectal NewDrugInformation |