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 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; RECTAL |
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: |
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ACTIVE STRENGTH: | 10(g/15mL) |
START MARKETING DATE: | 1995-07-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 50383-795_3649ca34-b4ac-4861-84b1-f8df74166e9d |
PRODUCT NDC: | 50383-795 |
APPLICATION NUMBER: | ANDA074077 |
Other LACTULOSE Pharmaceutical Manufacturers / Labelers: