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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lactulose
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LACTULOSE | 20 g/20g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9U7D5QH5AE |
| Rxcui | 1251190, 1251194 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69067-020-15 | Lactulose | 20 g in 1 PACKET | SOLUTION | 20 | | 9 |
| 69067-020-15 | Lactulose | 15 in 1 CARTON | SOLUTION | 15 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69067-020 | LACTULOSE SOLUTION [FOXLAND PHARMACEUTICALS, INC.] | 8 | Current NDC, 2 package rows | 20250426_3363bdbd-f0d1-45b3-8193-7fdb0a310cc2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |