Product NDC: | 0121-0577 |
Proprietary Name: | LACTULOSE |
Non Proprietary Name: | LACTULOSE |
Active Ingredient(s): | 10 g/15mL & nbsp; LACTULOSE |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0121-0577 |
Labeler Name: | Pharmaceutical Associates, Inc, |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074623 |
Marketing Category: | ANDA |
Start Marketing Date: | 19660730 |
Package NDC: | 0121-0577-16 |
Package Description: | 473 mL in 1 BOTTLE (0121-0577-16) |
NDC Code | 0121-0577-16 |
Proprietary Name | LACTULOSE |
Package Description | 473 mL in 1 BOTTLE (0121-0577-16) |
Product NDC | 0121-0577 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | LACTULOSE |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19660730 |
Marketing Category Name | ANDA |
Labeler Name | Pharmaceutical Associates, Inc, |
Substance Name | LACTULOSE |
Strength Number | 10 |
Strength Unit | g/15mL |
Pharmaceutical Classes | Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |