FDA NDC Directory · JSON-LD · Markdown
NDC 0078-0372 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE
| Generic name | methylphenidate hydrochloride |
|---|---|
| Labeler / Manufacturer | Novartis Pharmaceuticals Corporation |
| Marketing category | New Drug Application (innovator) · App NDA021284 |
| Dosage form / route | CAPSULE, EXTENDED RELEASE · ORAL |
| Active ingredients | METHYLPHENIDATE HYDROCHLORIDE (40 mg/1) |
| Marketing started | 20020605 |
| Marketing ended | 20261031 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).