ENEMEEZ Plus (Enemeez Inc. DBA Summit Pharmaceuticals)
Welcome to the PulseAid listing for the ENEMEEZ Plus drug offered from Enemeez Inc. DBA Summit Pharmaceuticals. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Enemeez Inc. DBA Summit Pharmaceuticals |
| NON-PROPRIETARY NAME: | DOCUSATE SODIUM and BENZOCAINE |
| SUBSTANCE NAME: | DOCUSATE SODIUM; BENZOCAINE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | RECTAL |
| DOSAGE FORM: | LIQUID |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2012-06-15 |
| END MARKETING DATE: | 0000-00-00 |
ENEMEEZ Plus HUMAN OTC DRUG Details:
| Item Description | ENEMEEZ Plus from Enemeez Inc. DBA Summit Pharmaceuticals |
| LABELER NAME: | Enemeez Inc. DBA Summit Pharmaceuticals |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 283; 20(mg/5mL; mg/5mL) |
| START MARKETING DATE: | 2012-06-15 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 17433-9877_a385116f-e477-4960-b91e-c15a558ba5d0 |
| PRODUCT NDC: | 17433-9877 |
| APPLICATION NUMBER: | part334 |
Other DOCUSATE SODIUM; BENZOCAINE Pharmaceutical Manufacturers / Labelers:
