M.V.I. Pediatric (Hospira, Inc.)
Welcome to the PulseAid listing for the M.V.I. Pediatric drug offered from Hospira, Inc.. This Ergocalciferols [Chemical/Ingredient],Provitamin D2 Compound [EPC],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Increased Prothrombin Activity [PE],Reversed Anticoagulation Activity [PE],Vitamin K [Chemical/Ingredient],Vitamin K [EPC],Warfarin Reversal Agent [EPC] 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: | ascorbic acid, retinol, ergocalciferol, thiamine hydrochloride, riboflavin 5-phosphate sodium, pyridoxine hydrochloride, niacinamide, dexpanthenol, .alpha.-tocopherol acetate, dl-, biotin, folic acid, |
SUBSTANCE NAME: | ASCORBIC ACID; RETINOL; ERGOCALCIFEROL; THIAMINE HYDROCHLORIDE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; PYRIDOXINE HYDROCHLORIDE; NIACINAMIDE; DEXPANTHENOL; .ALPHA.-TOCOPHEROL ACETATE, DL-; BIOTIN; FOLIC ACID |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Ergocalciferols [Chemical/Ingredient],Provitamin D2 Compound [EPC],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Increased Prothrombin Activity [PE],Reversed Anticoagulation Activity [PE],Vitamin K [Chemical/Ingredient],Vitamin K [EPC],Warfarin Reversal Agent [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2006-07-01 |
END MARKETING DATE: | 0000-00-00 |
M.V.I. Pediatric HUMAN PRESCRIPTION DRUG Details:
Item Description | M.V.I. Pediatric from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 80; .7; 10; 1.2; 1.4; 1; 17; 5; 7; 20; 140; 1; 200(mg/5mL; mg/5mL; ug/5mL; mg/5mL; mg/5mL; mg/5mL; mg/5mL; mg/5mL; mg/5mL; ug/5mL; ug/5mL; ug/5mL; ug/5mL) |
START MARKETING DATE: | 2006-07-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 61703-421_91e23adb-0710-40f7-b25f-eb97e41ae45d |
PRODUCT NDC: | 61703-421 |
APPLICATION NUMBER: | NDA018920 |
Other ASCORBIC ACID; RETINOL; ERGOCALCIFEROL; THIAMINE HYDROCHLORIDE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; PYRIDOXINE HYDROCHLORIDE; NIACINAMIDE; DEXPANTHENOL; .ALPHA.-TOCOPHEROL ACETATE, DL-; BIOTIN; FOLIC ACID Pharmaceutical Manufacturers / Labelers:
Manufacturer / Labeler | Proprietary Name |