NASOPENPE (GM Pharmaceuticals, Inc)
Welcome to the PulseAid listing for the NASOPEN drug offered from GM Pharmaceuticals, Inc. 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: | GM Pharmaceuticals, Inc |
| NON-PROPRIETARY NAME: | Phenylephrine Hydrochloride, Thonzylamine Hydrochloride |
| SUBSTANCE NAME: | PHENYLEPHRINE HYDROCHLORIDE; THONZYLAMINE HYDROCHLORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | LIQUID |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2012-10-03 |
| END MARKETING DATE: | 0000-00-00 |
NASOPEN PE HUMAN OTC DRUG Details:
| Item Description | NASOPEN PE from GM Pharmaceuticals, Inc |
| LABELER NAME: | GM Pharmaceuticals, Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10; 50(mg/15mL; mg/15mL) |
| START MARKETING DATE: | 2012-10-03 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 58809-729_44c2c20b-fdd4-41b4-b4f1-50131bb056b2 |
| PRODUCT NDC: | 58809-729 |
| APPLICATION NUMBER: | part341 |
Other PHENYLEPHRINE HYDROCHLORIDE; THONZYLAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
