Methazel (Sterling-Knight Pharmaceuticals, LLC)


Welcome to the PulseAid listing for the Methazel drug offered from Sterling-Knight Pharmaceuticals, LLC. This Antidote [EPC],Antidote for Acetaminophen Overdose [EPC],Decreased Respiratory Secretion Viscosity [PE],Increased Glutathione Concentration [PE],Mucolytic [EPC],Reduction Activity [MoA] 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: Sterling-Knight Pharmaceuticals, LLC
NON-PROPRIETARY NAME: Methazel
SUBSTANCE NAME: FOLIC ACID; PYRIDOXAL 5-PHOSPHATE; METHYLCOBALAMIN; COENZYME Q10, (2Z)-; ALPHA LIPOIC ACID; ACETYLCYSTEINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Antidote [EPC],Antidote for Acetaminophen Overdose [EPC],Decreased Respiratory Secretion Viscosity [PE],Increased Glutathione Concentration [PE],Mucolytic [EPC],Reduction Activity [MoA]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2015-10-12
END MARKETING DATE: 0000-00-00


Methazel HUMAN PRESCRIPTION DRUG Details:

Item DescriptionMethazel from Sterling-Knight Pharmaceuticals, LLC
LABELER NAME: Sterling-Knight Pharmaceuticals, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 50; 2.5; 25; 50; 50(mg/1; mg/1; mg/1; mg/1; mg/1; mg/1)
START MARKETING DATE: 2015-10-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 69336-350_9b74d855-bc07-4fa4-b48d-aafdff54343d
PRODUCT NDC: 69336-350
APPLICATION NUMBER:

Other FOLIC ACID; PYRIDOXAL 5-PHOSPHATE; METHYLCOBALAMIN; COENZYME Q10, (2Z)-; ALPHA LIPOIC ACID; ACETYLCYSTEINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Sterling-Knight Pharmaceuticals, LLCMethazel