LEADER RELIEF (HANLIM PHARM. CO., LTD.)
Welcome to the PulseAid listing for the LEADER RELIEF drug offered from HANLIM PHARM. CO., LTD.. 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: | HANLIM PHARM. CO., LTD. |
NON-PROPRIETARY NAME: | TETRAHYDROZOLINE HYDROCHLORIDE AND ZINC SULFATE |
SUBSTANCE NAME: | TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | SOLUTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2010-10-08 |
END MARKETING DATE: | 0000-00-00 |
LEADER RELIEF HUMAN OTC DRUG Details:
Item Description | LEADER RELIEF from HANLIM PHARM. CO., LTD. |
LABELER NAME: | HANLIM PHARM. CO., LTD. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | .5; 2.5(mg/mL; mg/mL) |
START MARKETING DATE: | 2010-10-08 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 11716-9638_7ccb006e-809f-4f34-9695-f4e93fc39f51 |
PRODUCT NDC: | 11716-9638 |
APPLICATION NUMBER: | part349 |
Other TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE Pharmaceutical Manufacturers / Labelers: