Dual Action Complete (H E B)
Welcome to the PulseAid listing for the Dual Action Complete drug offered from H E B. 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: | H E B |
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: | 2016-04-07 |
END MARKETING DATE: | 0000-00-00 |
Dual Action Complete HUMAN OTC DRUG Details:
Item Description | Dual Action Complete from H E B |
LABELER NAME: | H E B |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 10; 165; 800(mg/1; mg/1; mg/1) |
START MARKETING DATE: | 2016-04-07 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 37808-503_c1aa7efa-4be1-4c8f-8994-661dd60e1aa9 |
PRODUCT NDC: | 37808-503 |
APPLICATION NUMBER: | ANDA077355 |
Other FAMOTIDINE; MAGNESIUM HYDROXIDE; CALCIUM CARBONATE Pharmaceutical Manufacturers / Labelers: