Sunmark complete (McKesson)
Welcome to the PulseAid listing for the Sunmark complete 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: | famotidine, calcium carbonate and magnesium hydroxide |
SUBSTANCE NAME: | FAMOTIDINE; MAGNESIUM HYDROXIDE; CALCIUM CARBONATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, CHEWABLE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2012-12-04 |
END MARKETING DATE: | 0000-00-00 |
Sunmark complete HUMAN OTC DRUG Details:
Item Description | Sunmark complete from McKesson |
LABELER NAME: | McKesson |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 10; 165; 800(mg/1; mg/1; mg/1) |
START MARKETING DATE: | 2012-12-04 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 49348-403_c6b37ca6-7ce3-45fb-9815-c2b3b176cb54 |
PRODUCT NDC: | 49348-403 |
APPLICATION NUMBER: | ANDA077355 |
Other FAMOTIDINE; MAGNESIUM HYDROXIDE; CALCIUM CARBONATE Pharmaceutical Manufacturers / Labelers: