Package 68071-3563-3

Brand: ziprasidone hydrochloride

Generic: ziprasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3563-3
Digits Only 6807135633
Product NDC 68071-3563
Description

30 CAPSULE in 1 BOTTLE (68071-3563-3)

Marketing

Marketing Status
Marketed Since 2024-01-25
Brand ziprasidone hydrochloride
Generic ziprasidone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0fcead61-ddda-bcef-e063-6394a90af8a4", "openfda": {"upc": ["0368071356335"], "unii": ["216X081ORU"], "rxcui": ["313776"], "spl_set_id": ["0fcebd61-25b2-d287-e063-6394a90a7b9a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-3563-3)", "package_ndc": "68071-3563-3", "marketing_start_date": "20240125"}], "brand_name": "Ziprasidone Hydrochloride", "product_id": "68071-3563_0fcead61-ddda-bcef-e063-6394a90af8a4", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-3563", "generic_name": "Ziprasidone Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone Hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA204117", "marketing_category": "ANDA", "marketing_start_date": "20161227", "listing_expiration_date": "20261231"}