CODEINE AND CHLORPHENIRAMINE MALEATE ER (Nexgen Pharma, Inc.)


Welcome to the PulseAid listing for the CODEINE AND CHLORPHENIRAMINE MALEATE ER drug offered from Nexgen Pharma, Inc.. This Full Opioid Agonists [MoA],Opioid Agonist [EPC],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [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: Nexgen Pharma, Inc.
NON-PROPRIETARY NAME: CODEINE AND CHLORPHENIRAMINE MALEATE ER
SUBSTANCE NAME: CODEINE PHOSPHATE; CHLORPHENIRAMINE MALEATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Full Opioid Agonists [MoA],Opioid Agonist [EPC],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
ROUTE: ORAL
DOSAGE FORM: TABLET, EXTENDED RELEASE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2015-09-01
END MARKETING DATE: 0000-00-00


CODEINE AND CHLORPHENIRAMINE MALEATE ER HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCODEINE AND CHLORPHENIRAMINE MALEATE ER from Nexgen Pharma, Inc.
LABELER NAME: Nexgen Pharma, Inc.
DEA SCHEDULE: CIII
ACTIVE STRENGTH: 54.3; 8(mg/1; mg/1)
START MARKETING DATE: 2015-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0722-7184_6feb059d-5153-42a5-9306-6b05429ca86d
PRODUCT NDC: 0722-7184
APPLICATION NUMBER: NDA206323

Other CODEINE PHOSPHATE; CHLORPHENIRAMINE MALEATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Nexgen Pharma, Inc.CODEINE AND CHLORPHENIRAMINE MALEATE ER