Codeine Sulfate (Lannett Company, Inc.)
Welcome to the PulseAid listing for the Codeine Sulfate drug offered from Lannett Company, 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: | Lannett Company, Inc. |
| NON-PROPRIETARY NAME: | Codeine Sulfate |
| SUBSTANCE NAME: | CODEINE SULFATE |
| 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: | 2014-06-13 |
| END MARKETING DATE: | 0000-00-00 |
Codeine Sulfate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Codeine Sulfate from Lannett Company, Inc. |
| LABELER NAME: | Lannett Company, Inc. |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 30(mg/1) |
| START MARKETING DATE: | 2014-06-13 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0527-1698_2133b788-41c2-4fe0-9d4c-18942e9212ab |
| PRODUCT NDC: | 0527-1698 |
| APPLICATION NUMBER: | ANDA203046 |
Other CODEINE SULFATE Pharmaceutical Manufacturers / Labelers:
