ziprasidone
Generic: ziprasidone
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
ziprasidone
Generic Name
ziprasidone
Labeler
chartwell rx, llc
Dosage Form
CAPSULE
Routes
Active Ingredients
ziprasidone hydrochloride 80 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62135-994
Product ID
62135-994_02591199-8759-8e40-e063-6294a90afa7f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090348
Listing Expiration
2026-12-31
Marketing Start
2012-09-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135994
Hyphenated Format
62135-994
Supplemental Identifiers
RxCUI
UPC
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 (source: ndc)
Generic Name
ziprasidone (source: ndc)
Application Number
ANDA090348 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mg/1
Packaging
- 60 CAPSULE in 1 BOTTLE (62135-994-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "02591199-8759-8e40-e063-6294a90afa7f", "openfda": {"upc": ["0362135994600", "0362135992606", "0362135993603", "0362135991609"], "unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["7fbd9460-78a3-4160-9986-3a113de752a6"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (62135-994-60)", "package_ndc": "62135-994-60", "marketing_start_date": "20230428"}], "brand_name": "Ziprasidone", "product_id": "62135-994_02591199-8759-8e40-e063-6294a90afa7f", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "62135-994", "generic_name": "Ziprasidone", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA090348", "marketing_category": "ANDA", "marketing_start_date": "20120905", "listing_expiration_date": "20261231"}