NAT SULPH (Hyland’s)


Welcome to the PulseAid listing for the NAT SULPH 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: SODIUM SULFATE ANHYDROUS
SUBSTANCE NAME: SODIUM SULFATE ANHYDROUS
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 1940-01-01
END MARKETING DATE: 0000-00-00


NAT SULPH HUMAN OTC DRUG Details:

Item DescriptionNAT SULPH from Hyland’s
LABELER NAME: Hyland’s
DEA SCHEDULE:
ACTIVE STRENGTH: 30([hp_X]/1)
START MARKETING DATE: 1940-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54973-3111_2da837d5-263f-4b9a-b2be-7cf22eacf36b
PRODUCT NDC: 54973-3111
APPLICATION NUMBER:

Other SODIUM SULFATE ANHYDROUS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Hyland’sNAT SULPH