Chromium (Hospira, Inc.)
Welcome to the PulseAid listing for the Chromium 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: | Chromic Chloride |
SUBSTANCE NAME: | CHROMIC CHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2016-04-27 |
END MARKETING DATE: | 0000-00-00 |
Chromium HUMAN PRESCRIPTION DRUG Details:
Item Description | Chromium from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 4(ug/mL) |
START MARKETING DATE: | 2016-04-27 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0409-4093_18f76470-71f2-4a35-912a-cd923bfa6520 |
PRODUCT NDC: | 0409-4093 |
APPLICATION NUMBER: | NDA018961 |
Other CHROMIC CHLORIDE Pharmaceutical Manufacturers / Labelers: