Demerol (sanofi-aventis U.S. LLC)
Welcome to the PulseAid listing for the Demerol drug offered from sanofi-aventis U.S. LLC. 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: | sanofi-aventis U.S. LLC |
NON-PROPRIETARY NAME: | Meperidine Hydrochloride |
SUBSTANCE NAME: | MEPERIDINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1942-11-10 |
END MARKETING DATE: | 0000-00-00 |
Demerol HUMAN PRESCRIPTION DRUG Details:
Item Description | Demerol from sanofi-aventis U.S. LLC |
LABELER NAME: | sanofi-aventis U.S. LLC |
DEA SCHEDULE: | CII
|
ACTIVE STRENGTH: | 50(mg/1) |
START MARKETING DATE: | 1942-11-10 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0024-0335_4b1bd4df-00b7-4620-9dc5-bce675a412eb |
PRODUCT NDC: | 0024-0335 |
APPLICATION NUMBER: | NDA005010 |
Other MEPERIDINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: