Lactulose
NDC 68999-004, Lactulose, solution, from Chartwell Governmental & Specialty RX, LLC..
- Product NDC
- 68999-004
- Status
- Listed
- Labeler
- Chartwell Governmental & Specialty RX, LLC.
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209517
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68999-004 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LACTULOSE20 g/30mL
Pharmacologic classes
Acidifying Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68999-004-24 | 68999000424 | 2 TRAY in 1 BOX (68999-004-24) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (68999-004-43) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/887157ba-3c91-4fbf-bb12-b49c6fa4252c
Use it
Look up 68999-004 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68999-004 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68999-004. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.