Belladonna and Opium (Paddock Laboratories, LLC)


Welcome to the PulseAid listing for the Belladonna and Opium drug offered from Paddock Laboratories, LLC. 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: Paddock Laboratories, LLC
NON-PROPRIETARY NAME: ATROPA BELLADONNA and OPIUM
SUBSTANCE NAME: ATROPA BELLADONNA; OPIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: RECTAL
DOSAGE FORM: SUPPOSITORY
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 1997-04-22
END MARKETING DATE: 0000-00-00


Belladonna and Opium HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBelladonna and Opium from Paddock Laboratories, LLC
LABELER NAME: Paddock Laboratories, LLC
DEA SCHEDULE: CII
ACTIVE STRENGTH: 16.2; 60(mg/1; mg/1)
START MARKETING DATE: 1997-04-22
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0574-7040_eb1d764e-94f6-49aa-b6db-e1c5a2561256
PRODUCT NDC: 0574-7040
APPLICATION NUMBER:

Other ATROPA BELLADONNA; OPIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Paddock Laboratories, LLCBelladonna and Opium