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: