FDA NDC Directory · JSON-LD · Markdown
NDC 24338-855 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | Dextroamphetamine Sulfate |
|---|---|
| Labeler / Manufacturer | Azurity Pharmaceuticals, Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA090533 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | DEXTROAMPHETAMINE SULFATE (20 mg/1) |
| Marketing started | 20140501 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).