EMBEDA (Pfizer Laboratories Div Pfizer Inc)
Welcome to the PulseAid listing for the EMBEDA drug offered from Pfizer Laboratories Div Pfizer Inc. This Full Opioid Agonists [MoA],Opioid Agonist [EPC],Opioid Antagonist [EPC],Opioid Antagonists [MoA] 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: | Pfizer Laboratories Div Pfizer Inc |
| NON-PROPRIETARY NAME: | MORPHINE SULFATE and NALTREXONE HYDROCHLORIDE |
| SUBSTANCE NAME: | MORPHINE SULFATE; NALTREXONE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Full Opioid Agonists [MoA],Opioid Agonist [EPC],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2009-08-13 |
| END MARKETING DATE: | 0000-00-00 |
EMBEDA HUMAN PRESCRIPTION DRUG Details:
| Item Description | EMBEDA from Pfizer Laboratories Div Pfizer Inc |
| LABELER NAME: | Pfizer Laboratories Div Pfizer Inc |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 20; .8(mg/1; mg/1) |
| START MARKETING DATE: | 2009-08-13 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 60793-430_22852274-22cf-4619-9980-4ae3bc0ffdc6 |
| PRODUCT NDC: | 60793-430 |
| APPLICATION NUMBER: | NDA022321 |
Other MORPHINE SULFATE; NALTREXONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
