FDA NDC Directory · JSON-LD · Markdown
NDC 57664-643 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | Dextroamphetamine saccharate, Amphetamine aspartate, Dextroamphetamine sulfate, and Amphetamine sulfate |
|---|---|
| Labeler / Manufacturer | Sun Pharmaceutical Industries, Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA040480 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | AMPHETAMINE ASPARTATE (2.5 mg/1) AMPHETAMINE SULFATE (2.5 mg/1) DEXTROAMPHETAMINE SACCHARATE (2.5 mg/1) DEXTROAMPHETAMINE SULFATE (2.5 mg/1) |
| Marketing started | 20030909 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).