Benzonatate (Preferred Pharmaceuticals Inc.)


Welcome to the PulseAid listing for the Benzonatate drug offered from Preferred Pharmaceuticals Inc.. This Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [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: Preferred Pharmaceuticals Inc.
NON-PROPRIETARY NAME: Benzonatate
SUBSTANCE NAME: BENZONATATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2016-12-05
END MARKETING DATE: 0000-00-00


Benzonatate HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBenzonatate from Preferred Pharmaceuticals Inc.
LABELER NAME: Preferred Pharmaceuticals Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 200(mg/1)
START MARKETING DATE: 2016-12-05
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68788-6839_83409b37-916f-4522-a8e0-88fcf9c1932e
PRODUCT NDC: 68788-6839
APPLICATION NUMBER: ANDA202765

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