ziprasidone hydrochloride

Generic: ziprasidone hydrochloride

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ziprasidone hydrochloride
Generic Name ziprasidone hydrochloride
Labeler bluepoint laboratories
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ziprasidone hydrochloride 40 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-451
Product ID 68001-451_326cdd3c-c314-ff98-e063-6294a90a2a20
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204117
Listing Expiration 2026-12-31
Marketing Start 2020-08-31

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001451
Hyphenated Format 68001-451

Supplemental Identifiers

RxCUI
313776 313777 313778 314286
UPC
0368001450065
UNII
216X081ORU

Packaging Origin

Original Packager
true

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
  • 60 CAPSULE in 1 BOTTLE (68001-451-06)
source: ndc

Packages (1)

68001-451-06 60 CAPSULE in 1 BOTTLE (68001-451-06)

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": "326cdd3c-c314-ff98-e063-6294a90a2a20", "openfda": {"upc": ["0368001450065"], "unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["c0eb7b4d-0264-4eed-8756-51bba3af82fb"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (68001-451-06)", "package_ndc": "68001-451-06", "marketing_start_date": "20200831"}], "brand_name": "Ziprasidone Hydrochloride", "product_id": "68001-451_326cdd3c-c314-ff98-e063-6294a90a2a20", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68001-451", "generic_name": "Ziprasidone Hydrochloride", "labeler_name": "BluePoint Laboratories", "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": "20200831", "listing_expiration_date": "20261231"}