FDA NDC Directory · JSON-LD · Markdown

Cabergoline

NDC 70512-860 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namecabergoline
Labeler / ManufacturerSOLA Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076310
Dosage form / routeTABLET · ORAL
Active ingredientsCABERGOLINE (.5 mg/1)
Marketing started20230508
Package count1

External sources

Source: openFDA. Public-domain (CC0).