FDA NDC Directory · JSON-LD · Markdown
NDC 0310-3512 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | acalabrutinib |
|---|---|
| Labeler / Manufacturer | AstraZeneca Pharmaceuticals LP |
| Marketing category | New Drug Application (innovator) · App NDA216387 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | ACALABRUTINIB (100 mg/1) |
| Marketing started | 20220804 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).