NDC product
Sodium Phenylbutyrate
NDC 49884-006 · Par Health USA, LLC
Key facts
| Product NDC | 49884-006 |
|---|---|
| Proprietary name | Sodium Phenylbutyrate |
| Nonproprietary name | Sodium Phenylbutyrate |
| Substances | SODIUM PHENYLBUTYRATE |
| Dosage form | POWDER |
| Route | ORAL |
| Labeler | Par Health USA, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA203918 |
| Pharmacologic classes | Ammonium Ion Binding Activity [MoA], Nitrogen Binding Agent [EPC] |
| Marketing start | Aug 31, 2016 |
| 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: