Meperidine Hydrochloride (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Meperidine Hydrochloride drug offered from Teva Pharmaceuticals USA, 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: | Teva Pharmaceuticals USA, Inc. |
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: | ANDA |
START MARKETING DATE: | 1997-02-03 |
END MARKETING DATE: | 0000-00-00 |
Meperidine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Meperidine Hydrochloride from Teva Pharmaceuticals USA, Inc. |
LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
DEA SCHEDULE: | CII
|
ACTIVE STRENGTH: | 50(mg/1) |
START MARKETING DATE: | 1997-02-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0555-0381_7aac04b4-4adc-4c05-9892-23c13bf5fdb3 |
PRODUCT NDC: | 0555-0381 |
APPLICATION NUMBER: | ANDA088639 |
Other MEPERIDINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: