Lactulose 51672-4243
Product NDC
51672-4243- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 2, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA218858
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lactulose | 10 g/15mL |
Drug Class
Osmotic Laxative [EPC]Acidifying Activity [MoA]Osmotic Activity [MoA]
Packaging Options(1)
1 BOTTLE in 1 CARTON (51672-4243-9) / 473 mL in 1 BOTTLE