LACTULOSE (NuCare Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the LACTULOSE drug offered from NuCare 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: | NuCare 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: | SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1966-07-30 |
END MARKETING DATE: | 0000-00-00 |
LACTULOSE HUMAN PRESCRIPTION DRUG Details:
Item Description | LACTULOSE from NuCare Pharmaceuticals, Inc. |
LABELER NAME: | NuCare Pharmaceuticals, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(g/15mL) |
START MARKETING DATE: | 1966-07-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68071-1562_54255033-c2a2-042b-e054-00144ff8d46c |
PRODUCT NDC: | 68071-1562 |
APPLICATION NUMBER: | ANDA074623 |
Other LACTULOSE Pharmaceutical Manufacturers / Labelers: