Lactulose Solution is a Oral Solution in the Human Prescription Drug category. It is labeled and distributed by Slate Run Pharmaceuticals Llc. The primary component is Lactulose.
| Product ID | 70436-003_6f6e1fd5-b789-489d-a683-bd8b55965ed0 |
| NDC | 70436-003 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Lactulose Solution |
| Generic Name | Lactulose Solution |
| Dosage Form | Solution |
| Route of Administration | ORAL |
| Marketing Start Date | 2019-04-01 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA209517 |
| Labeler Name | Slate Run Pharmaceuticals LLC |
| Substance Name | LACTULOSE |
| Active Ingredient Strength | 10 g/15mL |
| Pharm Classes | Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2019-04-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA209517 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA209517 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA209517 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA209517 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA209517 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA209517 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| LACTULOSE | 10 g/15mL |
| SPL SET ID: | 6f6e1fd5-b789-489d-a683-bd8b55965ed0 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 61037-471 | Lactulose Solution | Lactulose Solution USP, 10 g/15 mL |
| 70436-003 | Lactulose Solution | Lactulose Solution |
| 80432-001 | Lactulose Solution | Lactulose Solution |