LORTUSSLQ (Poly Pharmaceuticals)
Welcome to the PulseAid listing for the LORTUSS drug offered from Poly 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: | Poly Pharmaceuticals |
| NON-PROPRIETARY NAME: | Doxylamine Succinate, Pseudoephedrine Hydrochloride |
| SUBSTANCE NAME: | DOXYLAMINE SUCCINATE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | LIQUID |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2011-02-22 |
| END MARKETING DATE: | 0000-00-00 |
LORTUSS LQ HUMAN OTC DRUG Details:
| Item Description | LORTUSS LQ from Poly Pharmaceuticals |
| LABELER NAME: | Poly Pharmaceuticals |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 6.25; 30(mg/5mL; mg/5mL) |
| START MARKETING DATE: | 2011-02-22 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50991-597_63857ec2-106a-4e39-bdc2-b15a4a0d3ff1 |
| PRODUCT NDC: | 50991-597 |
| APPLICATION NUMBER: | part341 |
Other DOXYLAMINE SUCCINATE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
