Acetaminophen and Codeine Phosphate (Sun Pharmaceutical Industries, Inc.)
Welcome to the PulseAid listing for the Acetaminophen and Codeine Phosphate drug offered from Sun Pharmaceutical Industries, 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: | Sun Pharmaceutical Industries, Inc. |
| NON-PROPRIETARY NAME: | Acetaminophen and Codeine Phosphate |
| SUBSTANCE NAME: | CODEINE PHOSPHATE; ACETAMINOPHEN |
| 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: | 1980-01-23 |
| END MARKETING DATE: | 0000-00-00 |
Acetaminophen and Codeine Phosphate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Acetaminophen and Codeine Phosphate from Sun Pharmaceutical Industries, Inc. |
| LABELER NAME: | Sun Pharmaceutical Industries, Inc. |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 60; 300(mg/1; mg/1) |
| START MARKETING DATE: | 1980-01-23 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63304-561_607ef64e-c16f-4433-85e1-092fff03bbab |
| PRODUCT NDC: | 63304-561 |
| APPLICATION NUMBER: | ANDA087083 |
Other CODEINE PHOSPHATE; ACETAMINOPHEN Pharmaceutical Manufacturers / Labelers:
