ziprasidone hydrochloride

Generic: ziprasidone hydrochloride

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ziprasidone hydrochloride
Generic Name ziprasidone hydrochloride
Labeler nucare pharmaceuticals,inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ziprasidone hydrochloride 40 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3563
Product ID 68071-3563_0fcead61-ddda-bcef-e063-6394a90af8a4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204117
Listing Expiration 2026-12-31
Marketing Start 2016-12-27

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713563
Hyphenated Format 68071-3563

Supplemental Identifiers

RxCUI
313776
UPC
0368071356335
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 ANDA204117 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (68071-3563-3)
source: ndc

Packages (1)

68071-3563-3 30 CAPSULE in 1 BOTTLE (68071-3563-3)

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": "0fcead61-ddda-bcef-e063-6394a90af8a4", "openfda": {"upc": ["0368071356335"], "unii": ["216X081ORU"], "rxcui": ["313776"], "spl_set_id": ["0fcebd61-25b2-d287-e063-6394a90a7b9a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-3563-3)", "package_ndc": "68071-3563-3", "marketing_start_date": "20240125"}], "brand_name": "Ziprasidone Hydrochloride", "product_id": "68071-3563_0fcead61-ddda-bcef-e063-6394a90af8a4", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-3563", "generic_name": "Ziprasidone Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone Hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA204117", "marketing_category": "ANDA", "marketing_start_date": "20161227", "listing_expiration_date": "20261231"}