AMBRA GRISEA (HOMEOLAB USA INC.)


Welcome to the PulseAid listing for the AMBRA GRISEA 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: AMBRA GRISEA
SUBSTANCE NAME: AMBERGRIS
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


AMBRA GRISEA HUMAN OTC DRUG Details:

Item DescriptionAMBRA GRISEA from HOMEOLAB USA INC.
LABELER NAME: HOMEOLAB USA INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 2([hp_X]/1)
START MARKETING DATE: 1995-10-11
END MARKETING DATE: 0000-00-00
PRODUCT ID: 60512-7101_cafb8adf-a8f6-46f1-8183-552091dffe21
PRODUCT NDC: 60512-7101
APPLICATION NUMBER:

Other AMBERGRIS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
HOMEOLAB USA INC.AMBRA GRISEA
Natural Health SupplyNervous Cough
Rxhomeo Private Limited d.b.a. Rxhomeo, IncAMBRA GRISEA
Washington Homeopathic ProductsAmbra grisea