NDC Code | 64980-592-12 |
Package Description | 118 mL in 1 BOTTLE (64980-592-12) |
Product NDC | 64980-592 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Lactulose Solution |
Non-Proprietary Name | Lactulose Solution Usp, 10 G/15 Ml |
Dosage Form | SOLUTION |
Usage | ORAL; RECTAL |
Start Marketing Date | 20211014 |
Marketing Category Name | ANDA |
Application Number | ANDA076645 |
Manufacturer | Rising Pharmaceuticals, Inc. |
Substance Name | LACTULOSE |
Strength | 10 |
Strength Unit | g/15mL |
Pharmacy Classes | Acidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |