ziprasidone hydrochloride
Generic: ziprasidone hcl
Labeler: golden state medical supply, inc.Drug Facts
Product Profile
Brand Name
ziprasidone hydrochloride
Generic Name
ziprasidone hcl
Labeler
golden state medical supply, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
ziprasidone hydrochloride 80 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60429-768
Product ID
60429-768_32fe222b-27ec-e636-e063-6294a90aa2ea
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077561
Listing Expiration
2026-12-31
Marketing Start
2012-03-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60429768
Hyphenated Format
60429-768
Supplemental Identifiers
RxCUI
UNII
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
- 80 mg/1
Packaging
- 60 CAPSULE in 1 BOTTLE (60429-768-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32fe222b-27ec-e636-e063-6294a90aa2ea", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["b1f52226-4fb4-48bf-8bfd-0c9df6ca02fa"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (60429-768-60)", "package_ndc": "60429-768-60", "marketing_start_date": "20120720"}], "brand_name": "ziprasidone hydrochloride", "product_id": "60429-768_32fe222b-27ec-e636-e063-6294a90aa2ea", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "60429-768", "generic_name": "Ziprasidone HCl", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA077561", "marketing_category": "ANDA", "marketing_start_date": "20120302", "listing_expiration_date": "20261231"}