OLOPATADINE HYDROCHLORIDE (Somerset Therapeutics, LLC)
Welcome to the PulseAid listing for the OLOPATADINE HYDROCHLORIDE drug offered from Somerset Therapeutics, LLC. This Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [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: | Somerset Therapeutics, LLC |
| NON-PROPRIETARY NAME: | OLOPATADINE HYDROCHLORIDE |
| SUBSTANCE NAME: | OLOPATADINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC] |
| ROUTE: | OPHTHALMIC |
| DOSAGE FORM: | SOLUTION/ DROPS |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-06-29 |
| END MARKETING DATE: | 0000-00-00 |
OLOPATADINE HYDROCHLORIDE HUMAN PRESCRIPTION DRUG Details:
| Item Description | OLOPATADINE HYDROCHLORIDE from Somerset Therapeutics, LLC |
| LABELER NAME: | Somerset Therapeutics, LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1.11(mg/mL) |
| START MARKETING DATE: | 2016-06-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 70069-007_f70f4372-fa89-4514-9763-8a2b7027756a |
| PRODUCT NDC: | 70069-007 |
| APPLICATION NUMBER: | ANDA206306 |
Other OLOPATADINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
