ziprasidone hydrochloride
Generic: ziprasidone hcl
Labeler: apotex corp.Drug Facts
Product Profile
Brand Name
ziprasidone hydrochloride
Generic Name
ziprasidone hcl
Labeler
apotex corp.
Dosage Form
CAPSULE
Routes
Active Ingredients
ziprasidone hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60505-2528
Product ID
60505-2528_a417f1c2-2445-61b8-9a00-df9371064e52
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077561
Listing Expiration
2026-12-31
Marketing Start
2012-05-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
605052528
Hyphenated Format
60505-2528
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ziprasidone hydrochloride (source: ndc)
Generic Name
ziprasidone hcl (source: ndc)
Application Number
ANDA077561 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 60 CAPSULE in 1 BOTTLE (60505-2528-6)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a417f1c2-2445-61b8-9a00-df9371064e52", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["ccfd5ba2-7271-f3dd-4c98-7418c1a4b54a"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (60505-2528-6)", "package_ndc": "60505-2528-6", "marketing_start_date": "20120514"}], "brand_name": "ziprasidone hydrochloride", "product_id": "60505-2528_a417f1c2-2445-61b8-9a00-df9371064e52", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "60505-2528", "generic_name": "Ziprasidone HCl", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA077561", "marketing_category": "ANDA", "marketing_start_date": "20120514", "listing_expiration_date": "20261231"}