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 Description | NAT 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: