OPIUM (Remedy Makers)


Welcome to the PulseAid listing for the OPIUM drug offered from Remedy Makers. This 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: Remedy Makers
NON-PROPRIETARY NAME: Raw Opium Gum
SUBSTANCE NAME: OPIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: SUBLINGUAL
DOSAGE FORM: PELLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2015-05-21
END MARKETING DATE: 0000-00-00


OPIUM HUMAN PRESCRIPTION DRUG Details:

Item DescriptionOPIUM from Remedy Makers
LABELER NAME: Remedy Makers
DEA SCHEDULE: CII
ACTIVE STRENGTH: 3([hp_X]/1)
START MARKETING DATE: 2015-05-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 10191-1081_19af6116-0298-3cfb-e054-00144ff8d46c
PRODUCT NDC: 10191-1081
APPLICATION NUMBER:

Other OPIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Paramesh Banerji Life Sciences LLCOpium 30C
Remedy MakersOPIUM