NDC 59148-047-90 - BUSULFEX

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC

59148-047

Requested NDC

59148-047-90

Package NDCs from labels

59148-047-90, 59148-047-91

Manufacturer

Otsuka America Pharmaceutical, Inc. | Galbraith Laboratories, Inc. | Eurofins Lancaster Laboratories, Inc | Avista Pharma Solutions, Inc. | Alcami Missouri Corporation | Sharp Corporation | Baxter Oncology GmbH | Mayne Pharma Inc.

Effective date

2020-04-16

Current FDA listing

Not matched in FDA.report NDC product tables