Ibuprofen and Diphenhydramine HCl (P and L Development of New York Corporation)
Welcome to the PulseAid listing for the Ibuprofen and Diphenhydramine HCl drug offered from P and 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 and L Development of New York Corporation |
NON-PROPRIETARY NAME: | IBUPROFEN, DIPHENHYDRAMINE HCL |
SUBSTANCE NAME: | IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE, LIQUID FILLED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2011-09-01 |
END MARKETING DATE: | 0000-00-00 |
Ibuprofen and Diphenhydramine HCl HUMAN OTC DRUG Details:
Item Description | Ibuprofen and Diphenhydramine HCl from P and L Development of New York Corporation |
LABELER NAME: | P and L Development of New York Corporation |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 200; 25(mg/1; mg/1) |
START MARKETING DATE: | 2011-09-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 59726-165_b2834fcc-cba7-41a7-9460-14755621b330 |
PRODUCT NDC: | 59726-165 |
APPLICATION NUMBER: | ANDA090397 |
Other IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: