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Hyperlyte
Hyperlyte - 0264-1943-20 - (Multi Electrolyte Concentrate)
Drug Information of Hyperlyte
| Product NDC: | 0264-1943 |
| Proprietary Name: | Hyperlyte |
| Non Proprietary Name: | Multi Electrolyte Concentrate |
| Active Ingredient(s): | .37; .51; 1.96; .68; 1.17 g/20mL; g/20mL; g/20mL; g/20mL; g/20mL & nbsp; Multi Electrolyte Concentrate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hyperlyte
| Product NDC: | 0264-1943 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120412 |
Package Information of Hyperlyte
| Package NDC: | 0264-1943-20 |
| Package Description: | 12 CONTAINER in 1 CASE (0264-1943-20) > 250 mL in 1 CONTAINER |
NDC Information of Hyperlyte
| NDC Code | 0264-1943-20 |
| Proprietary Name | Hyperlyte |
| Package Description | 12 CONTAINER in 1 CASE (0264-1943-20) > 250 mL in 1 CONTAINER |
| Product NDC | 0264-1943 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Multi Electrolyte Concentrate |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120412 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; SODIUM ACETATE; SODIUM CHLORIDE |
| Strength Number | .37; .51; 1.96; .68; 1.17 |
| Strength Unit | g/20mL; g/20mL; g/20mL; g/20mL; g/20mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient] |
