Tramadol Hydrochloride and Acetaminophen (Zydus Pharmaceuticals (USA) Inc.)
Welcome to the PulseAid listing for the Tramadol Hydrochloride and Acetaminophen drug offered from Zydus 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: | Zydus Pharmaceuticals (USA) Inc. |
NON-PROPRIETARY NAME: | Tramadol Hydrochloride and Acetaminophen |
SUBSTANCE NAME: | ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2012-10-15 |
END MARKETING DATE: | 0000-00-00 |
Tramadol Hydrochloride and Acetaminophen HUMAN PRESCRIPTION DRUG Details:
Item Description | Tramadol Hydrochloride and Acetaminophen from Zydus Pharmaceuticals (USA) Inc. |
LABELER NAME: | Zydus Pharmaceuticals (USA) Inc. |
DEA SCHEDULE: | CIV
|
ACTIVE STRENGTH: | 325; 37.5(mg/1; mg/1) |
START MARKETING DATE: | 2012-10-15 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68382-334_2182fa04-4d8a-4ce1-a027-1ae4ef9e1dbb |
PRODUCT NDC: | 68382-334 |
APPLICATION NUMBER: | ANDA090460 |
Other ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: