NDC product
Ursodiol 400 mg
NDC 79739-7144 · LGM PHARMA SOLUTIONS, LLC
Key facts
| Product NDC | 79739-7144 |
|---|---|
| Proprietary name | Ursodiol 400 mg |
| Nonproprietary name | Usodiol |
| Substances | URSODIOL |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | LGM PHARMA SOLUTIONS, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA205789 |
| Pharmacologic classes | Bile Acid [EPC], Bile Acids and Salts [CS] |
| Marketing start | Jul 1, 2020 |
| 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: