FDA NDC Directory · JSON-LD · Markdown

Colestipol Hydrochloride

NDC 42799-115 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA217667
Dosage form / routeTABLET · ORAL
Active ingredientsCOLESTIPOL HYDROCHLORIDE (1 g/1)
Marketing started20241126
Package count1

External sources

Source: openFDA. Public-domain (CC0).