Kristalose (Cumberland Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Kristalose drug offered from Cumberland Pharmaceuticals Inc.. This Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view the 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 PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Cumberland Pharmaceuticals Inc. |
NON-PROPRIETARY NAME: | lactulose |
SUBSTANCE NAME: | LACTULOSE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
ROUTE: | ORAL |
DOSAGE FORM: | POWDER, FOR SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2012-01-20 |
END MARKETING DATE: | 0000-00-00 |
Kristalose HUMAN PRESCRIPTION DRUG Details:
Item Description | Kristalose from Cumberland Pharmaceuticals Inc. |
LABELER NAME: | Cumberland Pharmaceuticals Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(g/10g) |
START MARKETING DATE: | 2012-01-20 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 66220-719_345383dc-2e49-462c-b304-d49c3be6783e |
PRODUCT NDC: | 66220-719 |
APPLICATION NUMBER: | ANDA074712 |
Other LACTULOSE Pharmaceutical Manufacturers / Labelers: