Product NDC: | 0054-8486 |
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: | 0054-8486 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA073591 |
Marketing Category: | ANDA |
Start Marketing Date: | 19920529 |
Package NDC: | 0054-8486-16 |
Package Description: | 40 CUP, UNIT-DOSE in 1 CONTAINER (0054-8486-16) > 30 mL in 1 CUP, UNIT-DOSE |
NDC Code | 0054-8486-16 |
Proprietary Name | Lactulose |
Package Description | 40 CUP, UNIT-DOSE in 1 CONTAINER (0054-8486-16) > 30 mL in 1 CUP, UNIT-DOSE |
Product NDC | 0054-8486 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lactulose |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19920529 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, 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] |