Lactulose
- Product NDC
- 50090-0679
- 11-digit product format
- 500900679
- Labeler code
- 50090
- Product ID
- 50090-0679_c28230dd-9040-427b-a8f5-71ea5df1ebe4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lactulose
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075993
- Marketing category
- ANDA
- Marketing start
- 2001-07-26
- Marketing end
- 0000-00-00
- Substance
- LACTULOSE
- Active strength
- 10 g/15mL
- Pharmacologic classes
- Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-0679-0 | Lactulose | 236 mL in 1 BOTTLE | SOLUTION | 236 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0679 | LACTULOSE SOLUTION [A-S MEDICATION SOLUTIONS] | 7 | Legacy NDC, 1 package rows | 20171019_9081e562-ce03-4781-a62d-e5a27320e096.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50090-0679-0 | 50090067900 | 236 mL in 1 BOTTLE | 236 ml | Historical |