Product NDC: | 0264-7704 |
Proprietary Name: | Isolyte S in Dextrose |
Non Proprietary Name: | Hydrous Dextrose, Sodium Chloride, Sodium Gluconate, Sodium Acetate Trihydrate, Potassium Chloride and Magnesium Chloride Hexahydrate |
Active Ingredient(s): | 5; .03; .037; .37; .53; .5 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; Hydrous Dextrose, Sodium Chloride, Sodium Gluconate, Sodium Acetate Trihydrate, Potassium Chloride and Magnesium Chloride Hexahydrate |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0264-7704 |
Labeler Name: | B. Braun Medical Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA019843 |
Marketing Category: | ANDA |
Start Marketing Date: | 19930809 |
Package NDC: | 0264-7704-00 |
Package Description: | 12 CONTAINER in 1 CASE (0264-7704-00) > 1000 mL in 1 CONTAINER |
NDC Code | 0264-7704-00 |
Proprietary Name | Isolyte S in Dextrose |
Package Description | 12 CONTAINER in 1 CASE (0264-7704-00) > 1000 mL in 1 CONTAINER |
Product NDC | 0264-7704 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydrous Dextrose, Sodium Chloride, Sodium Gluconate, Sodium Acetate Trihydrate, Potassium Chloride and Magnesium Chloride Hexahydrate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19930809 |
Marketing Category Name | ANDA |
Labeler Name | B. Braun Medical Inc. |
Substance Name | DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE |
Strength Number | 5; .03; .037; .37; .53; .5 |
Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |