| NDC Code | 68999-004-24 |
|---|
| Package Description | 2 TRAY in 1 BOX (68999-004-24) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (68999-004-43) |
|---|
| Product NDC | 68999-004 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lactulose |
|---|
| Non-Proprietary Name | Lactulose |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20181123 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA209517 |
|---|
| Manufacturer | Chartwell Governmental & Specialty RX, LLC. |
|---|
| Substance Name | LACTULOSE |
|---|
| Strength | 20 |
|---|
| Strength Unit | g/30mL |
|---|
| Pharmacy Classes | Acidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
|---|