M.V.I. Adult (Hospira, Inc.)
Welcome to the PulseAid listing for the M.V.I. Adult drug offered from Hospira, Inc.. This 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: | retinol, ergocalciferol, .alpha.-tocopherol acetate, dl-, phytonadione, ascorbic acid, niacinamide, riboflavin 5-phosphate sodium, thiamine hydrochloride, pyridoxine hydrochloride, dexpanthenol, bioti |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2004-07-15 |
END MARKETING DATE: | 2018-05-01 |
M.V.I. Adult HUMAN PRESCRIPTION DRUG Details:
Item Description | M.V.I. Adult from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2004-07-15 |
END MARKETING DATE: | 2018-05-01 |
PRODUCT ID: | 61703-422_0bb23e3f-484a-40c4-b725-f1a9a8e87214 |
PRODUCT NDC: | 61703-422 |
APPLICATION NUMBER: | NDA021625 |