FDA NDC Directory · JSON-LD · Markdown

Anagrelide

NDC 62135-313 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076683
Dosage form / routeCAPSULE · ORAL
Active ingredientsANAGRELIDE HYDROCHLORIDE ANHYDROUS (1 mg/1)
Marketing started20050418
Package count1

External sources

Source: openFDA. Public-domain (CC0).