FDA NDC Directory · JSON-LD · Markdown

Albendazole

NDC 42799-110 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA211117
Dosage form / routeTABLET · ORAL
Active ingredientsALBENDAZOLE (200 mg/1)
Marketing started20190517
Package count1

External sources

Source: openFDA. Public-domain (CC0).