FDA NDC Directory · JSON-LD · Markdown
NDC 42858-055 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE
| Generic name | DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, and AMPHETAMINE SULFATE |
|---|---|
| Labeler / Manufacturer | Rhodes Pharmaceuticals LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA210651 |
| Dosage form / route | CAPSULE, EXTENDED RELEASE · ORAL |
| Active ingredients | AMPHETAMINE ASPARTATE MONOHYDRATE (1.25 mg/1) AMPHETAMINE SULFATE (1.25 mg/1) DEXTROAMPHETAMINE SACCHARATE (1.25 mg/1) DEXTROAMPHETAMINE SULFATE (1.25 mg/1) |
| Marketing started | 20190822 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).