Lactated Ringers and Dextrose is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Sodium Chloride; Sodium Lactate; Potassium Chloride; Calcium Chloride; Dextrose Monohydrate.
| Product ID | 0409-7929_39230f8c-4492-4860-be1c-5a61f454cbcd |
| NDC | 0409-7929 |
| 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 | 2005-02-28 |
| Marketing End Date | 2021-03-01 |
| Marketing Category | NDA / NDA |
| Application Number | NDA017608 |
| Labeler Name | Hospira, Inc. |
| Substance Name | SODIUM CHLORIDE; SODIUM LACTATE; POTASSIUM CHLORIDE; CALCIUM CHLORIDE; DEXTROSE MONOHYDRATE |
| Active Ingredient Strength | 600 mg/100mL; mg/100mL; mg/100mL; mg/100mL; g/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 |
| Marketing Start Date | 2005-02-28 |
| Marketing End Date | 2021-03-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA017608 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-05-09 |
| Marketing Category | NDA |
| Application Number | NDA017608 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1975-08-13 |
| Marketing End Date | 1975-08-14 |
| Marketing Category | NDA |
| Application Number | NDA017608 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1975-08-13 |
| Marketing End Date | 1975-08-14 |
| Marketing Category | NDA |
| Application Number | NDA017608 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-02-28 |
| Ingredient | Strength |
|---|---|
| SODIUM CHLORIDE | 600 mg/100mL |
| SPL SET ID: | eb269566-5024-4495-fb86-db0339bd0488 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0338-0125 | Lactated Ringers and Dextrose | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE and DEXTROSE MONOHYDRATE |
| 0409-7929 | Lactated Ringers and Dextrose | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE |
| 0990-7929 | Lactated Ringers and Dextrose | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE |
| 51662-1229 | LACTATED RINGERS AND DEXTROSE | SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM CHLORIDE, DEXTROSE |
| 51662-1521 | LACTATED RINGERS AND DEXTROSE | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE |