Tussin DM CoughNighttime Maximum Strength (P & L Development, LLC)
Welcome to the PulseAid listing for the Tussin DM Cough drug offered from P & L Development, LLC. 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: | P & L Development, LLC |
NON-PROPRIETARY NAME: | Dextromethorphan HBr, Doxylamine succinate |
SUBSTANCE NAME: | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | LIQUID |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2016-09-30 |
END MARKETING DATE: | 0000-00-00 |
Tussin DM Cough Nighttime Maximum Strength HUMAN OTC DRUG Details:
Item Description | Tussin DM Cough Nighttime Maximum Strength from P & L Development, LLC |
LABELER NAME: | P & L Development, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 30; 12.5(mg/10mL; mg/10mL) |
START MARKETING DATE: | 2016-09-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 49580-0414_f51cc997-b2bf-4c12-80bf-dbea79963315 |
PRODUCT NDC: | 49580-0414 |
APPLICATION NUMBER: | part341 |
Other DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE Pharmaceutical Manufacturers / Labelers: