ACONITE NAPELLIS (Hyland’s)


Welcome to the PulseAid listing for the ACONITE NAPELLIS drug offered from Hyland’s. 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: Hyland’s
NON-PROPRIETARY NAME: ACONITUM NAPELLUS ROOT
SUBSTANCE NAME: ACONITUM NAPELLUS ROOT
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 1955-01-01
END MARKETING DATE: 0000-00-00


ACONITE NAPELLIS HUMAN OTC DRUG Details:

Item DescriptionACONITE NAPELLIS from Hyland’s
LABELER NAME: Hyland’s
DEA SCHEDULE:
ACTIVE STRENGTH: 6([hp_X]/1)
START MARKETING DATE: 1955-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54973-0600_4819322d-0098-4845-b9c4-d13ae0dd3e5a
PRODUCT NDC: 54973-0600
APPLICATION NUMBER:

Other ACONITUM NAPELLUS ROOT Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
HOMEOLAB USA INC.ACONITUM, RADIX
Hyland’sACONITE NAPELLIS
Washington Homeopathic ProductsAconitum, radix