LACTULOSE
- Product NDC
- 55700-892
- 11-digit product format
- 557000892
- Labeler code
- 55700
- Product ID
- 55700-892_50b467c9-e112-457d-bf2e-aadf876bff07
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lactulose
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA074623
- Marketing category
- ANDA
- Marketing start
- 2021-01-22
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-892 | LACTULOSE SOLUTION [QUALITY CARE PRODUCTS, LLC] | 3 | Legacy NDC | 20241220_4089ccd2-e58d-4d2b-a9f0-40fcd9aaf615.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-892-32 | 55700089232 | 946 mL in 1 BOTTLE (55700-892-32) | 946 ml | 2021-01-22 | 0000-00-00 | No | No | Current |