Ringers (Hospira, Inc.)
Welcome to the PulseAid listing for the Ringers drug offered from Hospira, Inc.. This Potassium Compounds [Chemical/Ingredient],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 [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Hospira, Inc. |
| NON-PROPRIETARY NAME: | SODIUM CHLORIDE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE |
| SUBSTANCE NAME: | POTASSIUM CHLORIDE; CALCIUM CHLORIDE; SODIUM CHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Potassium Compounds [Chemical/Ingredient],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 [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1980-05-16 |
| END MARKETING DATE: | 0000-00-00 |
Ringers HUMAN PRESCRIPTION DRUG Details:
| Item Description | Ringers from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 30; 33; 860(mg/100mL; mg/100mL; mg/100mL) |
| START MARKETING DATE: | 1980-05-16 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-7982_c1916a1b-6b4b-450c-8ce6-ab05556cb979 |
| PRODUCT NDC: | 0409-7982 |
| APPLICATION NUMBER: | NDA018251 |
Other POTASSIUM CHLORIDE; CALCIUM CHLORIDE; SODIUM CHLORIDE Pharmaceutical Manufacturers / Labelers:
