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:
