Stool Softener (P & L Development of New York Corporation)
Welcome to the PulseAid listing for the Stool Softener drug offered from P & L Development of New York Corporation. 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: | P & L Development of New York Corporation |
NON-PROPRIETARY NAME: | DOCUSATE CALCIUM |
SUBSTANCE NAME: | DOCUSATE CALCIUM |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE, LIQUID FILLED |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2011-12-01 |
END MARKETING DATE: | 0000-00-00 |
Stool Softener HUMAN OTC DRUG Details:
Item Description | Stool Softener from P & L Development of New York Corporation |
LABELER NAME: | P & L Development of New York Corporation |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 240(mg/1) |
START MARKETING DATE: | 2011-12-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 59726-170_8632dcea-d09e-46be-8cf9-4dfc686f35d7 |
PRODUCT NDC: | 59726-170 |
APPLICATION NUMBER: | part334 |
Other DOCUSATE CALCIUM Pharmaceutical Manufacturers / Labelers: