LACTULOSE
- Product NDC
- 68071-1562
- 11-digit product format
- 680711562
- Labeler code
- 68071
- Product ID
- 68071-1562_d592eb64-38cf-749b-e053-2a95a90a3531
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LACTULOSE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA074623
- Marketing category
- ANDA
- Marketing start
- 1966-07-30
- Marketing end
- 0000-00-00
- Substance
- LACTULOSE
- Active strength
- 10 g/15mL
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1562-6 | 68071156206 | 473 mL in 1 BOTTLE (68071-1562-6) | 473 ml | 2017-07-12 | 0000-00-00 | No | No | Current |