Phentermine ResinER (Lannett Company, Inc.)


Welcome to the PulseAid listing for the Phentermine Resin drug offered from Lannett Company, Inc.. This Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [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: Lannett Company, Inc.
NON-PROPRIETARY NAME: Phentermine Resin
SUBSTANCE NAME: PHENTERMINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
ROUTE: ORAL
DOSAGE FORM: CAPSULE, EXTENDED RELEASE
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2011-07-28
END MARKETING DATE: 0000-00-00


Phentermine Resin ER HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPhentermine Resin ER from Lannett Company, Inc.
LABELER NAME: Lannett Company, Inc.
DEA SCHEDULE: CIV
ACTIVE STRENGTH: 30(mg/1)
START MARKETING DATE: 2011-07-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0527-1366_7bbef403-d696-4690-a1b1-8fd2d48eb52e
PRODUCT NDC: 0527-1366
APPLICATION NUMBER: ANDA040872

Other PHENTERMINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Lannett Company, Inc.Phentermine Resin