Lactulose (Hi-Tech Pharmacal Co., Inc.)
Welcome to the PulseAid listing for the Lactulose drug offered from Hi-Tech Pharmacal Co., 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: | Hi-Tech Pharmacal Co., 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: | 1995-07-03 |
| END MARKETING DATE: | 0000-00-00 |
Lactulose HUMAN PRESCRIPTION DRUG Details:
| Item Description | Lactulose from Hi-Tech Pharmacal Co., Inc. |
| LABELER NAME: | Hi-Tech Pharmacal Co., Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 10(g/15mL) |
| START MARKETING DATE: | 1995-07-03 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50383-779_2a039f04-91df-492f-ab04-f9b85d1f3caa |
| PRODUCT NDC: | 50383-779 |
| APPLICATION NUMBER: | ANDA074076 |
Other LACTULOSE Pharmaceutical Manufacturers / Labelers:
