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Lactulose
Lactulose - 17856-1378-1 - (lactulose)
Drug Information of Lactulose
| Product NDC: | 17856-1378 |
| 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) |
Labeler Information of Lactulose
| Product NDC: | 17856-1378 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075993 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010726 |
Package Information of Lactulose
| Package NDC: | 17856-1378-1 |
| Package Description: | 30 mL in 1 CUP (17856-1378-1) |
NDC Information of Lactulose
| NDC Code | 17856-1378-1 |
| Proprietary Name | Lactulose |
| Package Description | 30 mL in 1 CUP (17856-1378-1) |
| Product NDC | 17856-1378 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lactulose |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20010726 |
| Marketing Category Name | ANDA |
| Labeler Name | Atlantic Biologicals Corps |
| 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] |
