ACETAMINOPHEN (Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals)
Welcome to the PulseAid listing for the ACETAMINOPHEN drug offered from Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals. 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: | Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals |
NON-PROPRIETARY NAME: | ACETAMINOPHEN |
SUBSTANCE NAME: | ACETAMINOPHEN |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2012-03-30 |
END MARKETING DATE: | 0000-00-00 |
ACETAMINOPHEN HUMAN OTC DRUG Details:
Item Description | ACETAMINOPHEN from Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals |
LABELER NAME: | Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | 325(mg/1) |
START MARKETING DATE: | 2012-03-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51645-600_d62b9994-c87c-4671-a8bf-f70f117039bc |
PRODUCT NDC: | 51645-600 |
APPLICATION NUMBER: | part343 |