Sunmark All Day Allergy D (McKesson)
Welcome to the PulseAid listing for the Sunmark All Day Allergy D drug offered from McKesson. 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: | McKesson |
NON-PROPRIETARY NAME: | Cetirizine HCl, Pseudoephedrine HCl |
SUBSTANCE NAME: | CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2008-04-18 |
END MARKETING DATE: | 0000-00-00 |
Sunmark All Day Allergy D HUMAN OTC DRUG Details:
Item Description | Sunmark All Day Allergy D from McKesson |
LABELER NAME: | McKesson |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 5; 120(mg/1; mg/1) |
START MARKETING DATE: | 2008-04-18 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 49348-851_0cabdccd-5d24-40fe-a004-5ad4b5379718 |
PRODUCT NDC: | 49348-851 |
APPLICATION NUMBER: | ANDA077170 |
Other CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: