FDA NDC Directory · JSON-LD · Markdown

Tinidazole

NDC 42799-208 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA203808
Dosage form / routeTABLET · ORAL
Active ingredientsTINIDAZOLE (500 mg/1)
Marketing started20191220
Package count2

External sources

Source: openFDA. Public-domain (CC0).