FDA NDC Directory · JSON-LD · Markdown

Ziprasidone Hydrochloride

NDC 65862-704 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA204117
Dosage form / routeCAPSULE · ORAL
Active ingredientsZIPRASIDONE HYDROCHLORIDE (60 mg/1)
Marketing started20161227
Package count3

External sources

Source: openFDA. Public-domain (CC0).