NDC product
Buphenyl
NDC 75987-070 · Horizon Therapeutics USA, Inc.
Key facts
| Product NDC | 75987-070 |
|---|---|
| Proprietary name | Buphenyl |
| Nonproprietary name | sodium phenylbutyrate |
| Substances | SODIUM PHENYLBUTYRATE |
| Dosage form | POWDER |
| Route | ORAL |
| Labeler | Horizon Therapeutics USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA020573 |
| Pharmacologic classes | Ammonium Ion Binding Activity [MoA], Nitrogen Binding Agent [EPC] |
| Marketing start | Apr 30, 1996 |
| Listing certified through | Dec 31, 2026 |
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: