LACTULOSE
- Product NDC
- 55154-5775
- 11-digit product format
- 551545775
- Labeler code
- 55154
- Product ID
- 55154-5775_2e5f9e8e-ee89-4a73-ae9e-6ddbba0f0d10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LACTULOSE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA074623
- Marketing category
- ANDA
- Marketing start
- 1966-07-30
- Marketing end
- 2021-05-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-5775-5 | 55154577505 | 5 CUP, UNIT-DOSE in 1 BAG (55154-5775-5) > 30 mL in 1 CUP, UNIT-DOSE | 1966-07-30 | 2021-05-31 | No | No | Current |