ziprasidone hydrochloride
Generic: ziprasidone hydrochloride
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
ziprasidone hydrochloride
Generic Name
ziprasidone hydrochloride
Labeler
proficient rx lp
Dosage Form
CAPSULE
Routes
Active Ingredients
ziprasidone hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63187-168
Product ID
63187-168_67b8d9a0-2da1-4a8d-8775-ecbe065870d4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077562
Listing Expiration
2026-12-31
Marketing Start
2013-02-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63187168
Hyphenated Format
63187-168
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 hydrochloride (source: ndc)
Application Number
ANDA077562 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (63187-168-30)
- 60 CAPSULE in 1 BOTTLE (63187-168-60)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "67b8d9a0-2da1-4a8d-8775-ecbe065870d4", "openfda": {"unii": ["216X081ORU"], "rxcui": ["314286"], "spl_set_id": ["b650e8b6-6df7-4301-837d-3d3b650b7456"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (63187-168-30)", "package_ndc": "63187-168-30", "marketing_start_date": "20190101"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (63187-168-60)", "package_ndc": "63187-168-60", "marketing_start_date": "20190101"}], "brand_name": "ziprasidone hydrochloride", "product_id": "63187-168_67b8d9a0-2da1-4a8d-8775-ecbe065870d4", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "63187-168", "generic_name": "ziprasidone hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA077562", "marketing_category": "ANDA", "marketing_start_date": "20130213", "listing_expiration_date": "20261231"}