NATRUM SULPHURICUM (HOMEOLAB USA INC)
Welcome to the PulseAid listing for the NATRUM SULPHURICUM 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: | NATRUM SULPHURICUM |
SUBSTANCE NAME: | SODIUM SULFATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, CHEWABLE |
MARKETING CATEGORY NAME: | UNAPPROVED HOMEOPATHIC |
START MARKETING DATE: | 2014-03-25 |
END MARKETING DATE: | 0000-00-00 |
NATRUM SULPHURICUM HUMAN OTC DRUG Details:
Item Description | NATRUM SULPHURICUM from HOMEOLAB USA INC |
LABELER NAME: | HOMEOLAB USA INC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 6([hp_X]/1) |
START MARKETING DATE: | 2014-03-25 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 60512-8031_73e128ba-b414-4d87-89f6-b5ee06032d6a |
PRODUCT NDC: | 60512-8031 |
APPLICATION NUMBER: | |
Other SODIUM SULFATE Pharmaceutical Manufacturers / Labelers: