Ionosol MB 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 Dextrose Monohydrate; Sodium Lactate; Potassium Chloride; Magnesium Chloride; Potassium Phosphate, Monobasic; Sodium Phosphate, Monobasic, Monohydrate.
Product ID | 0409-7372_537a1775-b206-47cd-a2b8-29ef05f1fa1e |
NDC | 0409-7372 |
Product Type | Human Prescription Drug |
Proprietary Name | Ionosol MB and Dextrose |
Generic Name | Dextrose Monohydrate, Sodium Lactate, Potassium Chloride, Magnesium Chloride, Potassium Phosphate, Monobasic, And Sodium Phosphate, Monobasic, Monohydrate |
Dosage Form | Injection, Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2005-04-30 |
Marketing Category | NDA / NDA |
Application Number | NDA019513 |
Labeler Name | Hospira, Inc. |
Substance Name | DEXTROSE MONOHYDRATE; SODIUM LACTATE; POTASSIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
Active Ingredient Strength | 5 g/100mL; mg/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],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Potassium Compounds [CS],Potassium Salt [EPC],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] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2005-08-12 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA019513 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-05-04 |
Marketing End Date | 2011-05-05 |
Marketing Category | NDA |
Application Number | NDA019513 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-05-04 |
Marketing End Date | 2011-05-05 |
Marketing Category | NDA |
Application Number | NDA019513 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2005-04-30 |
Marketing Category | NDA |
Application Number | NDA019513 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2005-08-12 |
Marketing Category | NDA |
Application Number | NDA019513 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-05-04 |
Marketing End Date | 2011-05-05 |
Marketing Category | NDA |
Application Number | NDA019513 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2005-04-30 |
Marketing End Date | 2011-04-01 |
Ingredient | Strength |
---|---|
DEXTROSE MONOHYDRATE | 5 g/100mL |
SPL SET ID: | 207aab2b-4be1-4629-ffb5-5481e2ad534f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0409-7372 | Ionosol MB and Dextrose | DEXTROSE MONOHYDRATE, SODIUM LACTATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, POTASSIUM PHOSPHATE, MONOBASIC, and SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
0990-7372 | Ionosol MB and Dextrose | DEXTROSE MONOHYDRATE, SODIUM LACTATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, POTASSIUM PHOSPHATE, MONOBASIC, and SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |