Product ID | 51662-1521_a62cf623-9b8b-37e0-e053-2995a90add5b |
NDC | 51662-1521 |
Product Type | Human Prescription Drug |
Proprietary Name | LACTATED RINGERS AND DEXTROSE |
Generic Name | Sodium Chloride, Sodium Lactate, Potassium Chloride, Calcium Chloride, And Dextrose Monohydrate |
Dosage Form | Injection, Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2020-05-21 |
Marketing Category | NDA / NDA |
Application Number | NDA017608 |
Labeler Name | HF Acquisition Co LLC, DBA HealthFirst |
Substance Name | DEXTROSE MONOHYDRATE; SODIUM LACTATE; SODIUM CHLORIDE; POTASSIUM CHLORIDE; CALCIUM CHLORIDE |
Active Ingredient Strength | 5 g/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL |
Pharm Classes | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |