Modafinil (APPCO PHARMA LLC)
Welcome to the PulseAid listing for the Modafinil drug offered from APPCO PHARMA LLC. This Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [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: | APPCO PHARMA LLC |
NON-PROPRIETARY NAME: | Modafinil |
SUBSTANCE NAME: | MODAFINIL |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2017-11-01 |
END MARKETING DATE: | 0000-00-00 |
Modafinil HUMAN PRESCRIPTION DRUG Details:
Item Description | Modafinil from APPCO PHARMA LLC |
LABELER NAME: | APPCO PHARMA LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 100(mg/1) |
START MARKETING DATE: | 2017-11-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 55801-132_2937dd24-471b-409a-8868-45376b8ed417 |
PRODUCT NDC: | 55801-132 |
APPLICATION NUMBER: | ANDA207196 |
Other MODAFINIL Pharmaceutical Manufacturers / Labelers: