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Sodium SuccinateDrug - Sodium Succinate The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
Active Ingredient(s) -
Sodium Succinate
Strength -
30%
Applicant -
ELKINS SINN
New Drug Application (NDA) Number -
080516
Product Number -
001
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
Sodium Succinate
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 Sodium Phosphate P 32 1.5mci/vial Solution; Injection, Oral Kayexalate 453.6gm/bot Powder; Oral, Rectal Kionex 454gm/bot Powder; Oral, Rectal Sodium Polystyrene Sulfonate 454gm/bot Powder; Oral, Rectal Sodium Polystyrene Sulfonate 453.6gm/bot Powder; Oral, Rectal Sodium Polystyrene Sulfonate 15gm/60ml Suspension; Oral, Rectal NewDrugInformation |