NDC 43826-067 - Bupropion Hydrochloride (XL)

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

43826-067

Package NDCs from labels

43826-067-09, 43826-067-03, 43826-067-02

Manufacturer

Bora Pharmaceutical Laboratories Inc. | TWi Pharmaceuticals, Inc. Zhongli Plant

Effective date

2024-01-22

Current FDA listing

Not matched in FDA.report NDC product tables