ziprasidone hydrochloride

Generic: ziprasidone hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ziprasidone hydrochloride
Generic Name ziprasidone hydrochloride
Labeler a-s medication solutions
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ziprasidone hydrochloride 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5420
Product ID 50090-5420_a6511c1c-9700-4ce2-9ca2-f10cd1c96124
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204375
Listing Expiration 2026-12-31
Marketing Start 2017-02-18

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905420
Hyphenated Format 50090-5420

Supplemental Identifiers

RxCUI
313776
UNII
216X081ORU

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 ANDA204375 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE (50090-5420-0)
source: ndc

Packages (1)

50090-5420-0 60 CAPSULE in 1 BOTTLE (50090-5420-0)

Ingredients (1)

ziprasidone hydrochloride (40 mg/1)

Linked Drug Pages (1)

Ziprasidone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a6511c1c-9700-4ce2-9ca2-f10cd1c96124", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313776"], "spl_set_id": ["c3797145-cead-4fc4-9711-8b8623bb09f4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (50090-5420-0)", "package_ndc": "50090-5420-0", "marketing_start_date": "20210105"}], "brand_name": "Ziprasidone Hydrochloride", "product_id": "50090-5420_a6511c1c-9700-4ce2-9ca2-f10cd1c96124", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50090-5420", "generic_name": "Ziprasidone Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone Hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA204375", "marketing_category": "ANDA", "marketing_start_date": "20170218", "listing_expiration_date": "20261231"}