FDA NDC Directory · JSON-LD · Markdown
NDC 70165-015 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING
| Generic name | Amphetamine |
|---|---|
| Labeler / Manufacturer | Neos Therapeutics Brands, LLC |
| Marketing category | New Drug Application (innovator) · App NDA204326 |
| Dosage form / route | TABLET, ORALLY DISINTEGRATING · ORAL |
| Active ingredients | AMPHETAMINE (9.4 mg/1) |
| Marketing started | 20160216 |
| Package count | 1 |
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