Lactulose
- Product NDC
- 69067-020
- 11-digit product format
- 690670020
- Labeler code
- 69067
- Product ID
- 69067-020_4618824a-2b40-3d54-e063-6394a90a4b96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lactulose
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Foxland Pharmaceuticals, Inc.
- Application
- ANDA074712
- Marketing category
- ANDA
- Marketing start
- 2025-02-07
- Substance
- LACTULOSE
- Active strength
- 20 g/20g
- Pharmacologic classes
- Acidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9U7D5QH5AE | LACTULOSE | 4618-18-2 | LACTULOSE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69067-020-15 | 69067002015 | 15 PACKET in 1 CARTON (69067-020-15) / 20 g in 1 PACKET | 15 packet | 2025-02-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LACTULOSE For Oral Solution | Foxland Pharmaceuticals, Inc. | 2025-12-16 | HUMAN PRESCRIPTION DRUG LABEL | 9 |