Meperidine Hydrochloride (Hospira, Inc.)
Welcome to the PulseAid listing for the Meperidine Hydrochloride drug offered from Hospira, Inc.. This Full Opioid Agonists [MoA],Opioid Agonist [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: | Meperidine Hydrochloride |
SUBSTANCE NAME: | MEPERIDINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2005-09-02 |
END MARKETING DATE: | 0000-00-00 |
Meperidine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Meperidine Hydrochloride from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: | CII
|
ACTIVE STRENGTH: | 10(mg/mL) |
START MARKETING DATE: | 2005-09-02 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0409-6030_8c6e7b1a-3ee2-4ece-a862-5c94098e52c4 |
PRODUCT NDC: | 0409-6030 |
APPLICATION NUMBER: | ANDA088432 |
Other MEPERIDINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: