ALLIUM SATIVUM (HOMEOLAB USA INC.)


Welcome to the PulseAid listing for the ALLIUM SATIVUM drug offered from HOMEOLAB USA INC.. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: HOMEOLAB USA INC.
NON-PROPRIETARY NAME: ALLIUM SATIVUM
SUBSTANCE NAME: ALLIUM SATIVUM WHOLE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: PELLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 1995-10-11
END MARKETING DATE: 0000-00-00


ALLIUM SATIVUM HUMAN OTC DRUG Details:

Item DescriptionALLIUM SATIVUM from HOMEOLAB USA INC.
LABELER NAME: HOMEOLAB USA INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 1([hp_X]/1)
START MARKETING DATE: 1995-10-11
END MARKETING DATE: 0000-00-00
PRODUCT ID: 60512-6472_1e03e993-b0ac-47d3-8244-f879648c9c1c
PRODUCT NDC: 60512-6472
APPLICATION NUMBER:

Other ALLIUM SATIVUM WHOLE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
HOMEOLAB USA INC.ALLIUM SATIVUM