FDA NDC Directory · JSON-LD · Markdown
NDC 64764-543 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
| Generic name | lansoprazole |
|---|---|
| Labeler / Manufacturer | Takeda Pharmaceuticals America, Inc. |
| Marketing category | New Drug Application (innovator) · App NDA021428 |
| Dosage form / route | TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE · ORAL |
| Active ingredients | LANSOPRAZOLE (15 mg/1) |
| Marketing started | 20020830 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).