NDC product
Lactulose Solution
NDC 81033-241 · Kesin Pharma Corporation
Key facts
| Product NDC | 81033-241 |
|---|---|
| Proprietary name | Lactulose Solution |
| Nonproprietary name | Lactulose Solution USP, 10 g/15 mL |
| Substances | LACTULOSE |
| Dosage form | SOLUTION |
| Route | ORAL, RECTAL |
| Labeler | Kesin Pharma Corporation |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA076645 |
| Pharmacologic classes | Acidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
| Marketing start | Apr 16, 2021 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: