Lactulose
- Product NDC
- 49999-800
- 11-digit product format
- 499990800
- Labeler code
- 49999
- Product ID
- 49999-800_cc412b45-fbdb-4015-90ae-20938747fc4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lactulose
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA074623
- Marketing category
- ANDA
- Marketing start
- 2004-04-19
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49999-800-32 | 49999080032 | 946 mL in 1 BOTTLE (49999-800-32) | 946 ml | 2004-04-19 | 0000-00-00 | No | No | Current |