ziprasidone hydrochloride

Generic: ziprasidone hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ziprasidone hydrochloride
Generic Name ziprasidone hydrochloride
Labeler aurobindo pharma limited
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ziprasidone hydrochloride 60 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-704
Product ID 65862-704_7f518739-d6ea-4630-b7d5-45d78499149e
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 65862704
Hyphenated Format 65862-704

Supplemental Identifiers

RxCUI
313776 313777 313778 314286
UPC
0365862702609
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
  • 60 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE (65862-704-60)
  • 8 BLISTER PACK in 1 CARTON (65862-704-80) / 10 CAPSULE in 1 BLISTER PACK (65862-704-10)
  • 1000 CAPSULE in 1 BOTTLE (65862-704-99)
source: ndc

Packages (3)

65862-704-60 60 CAPSULE in 1 BOTTLE (65862-704-60) 65862-704-80 8 BLISTER PACK in 1 CARTON (65862-704-80) / 10 CAPSULE in 1 BLISTER PACK (65862-704-10) 65862-704-99 1000 CAPSULE in 1 BOTTLE (65862-704-99)

Ingredients (1)

ziprasidone hydrochloride (60 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": "7f518739-d6ea-4630-b7d5-45d78499149e", "openfda": {"upc": ["0365862702609"], "unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["cc5e1c44-79e9-45d3-b1e5-b003f550c508"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (65862-704-60)", "package_ndc": "65862-704-60", "marketing_start_date": "20161227"}, {"sample": false, "description": "8 BLISTER PACK in 1 CARTON (65862-704-80)  / 10 CAPSULE in 1 BLISTER PACK (65862-704-10)", "package_ndc": "65862-704-80", "marketing_start_date": "20161227"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (65862-704-99)", "package_ndc": "65862-704-99", "marketing_start_date": "20161227"}], "brand_name": "Ziprasidone Hydrochloride", "product_id": "65862-704_7f518739-d6ea-4630-b7d5-45d78499149e", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "65862-704", "generic_name": "Ziprasidone Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone Hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA204117", "marketing_category": "ANDA", "marketing_start_date": "20161227", "listing_expiration_date": "20261231"}