ziprasidone

Generic: ziprasidone

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ziprasidone
Generic Name ziprasidone
Labeler northstar rx llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ziprasidone hydrochloride 80 mg/1

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 16714-838
Product ID 16714-838_cbe5f617-d390-54a0-2849-585abd37300f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077565
Listing Expiration 2026-12-31
Marketing Start 2018-07-26

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16714838
Hyphenated Format 16714-838

Supplemental Identifiers

RxCUI
313776 313777 313778 314286
UPC
0316714836010 0316714835013
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 (source: ndc)
Generic Name ziprasidone (source: ndc)
Application Number ANDA077565 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE (16714-838-01)
source: ndc

Packages (1)

16714-838-01 60 CAPSULE in 1 BOTTLE (16714-838-01)

Ingredients (1)

ziprasidone hydrochloride (80 mg/1)

Linked Drug Pages (1)

ziprasidone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cbe5f617-d390-54a0-2849-585abd37300f", "openfda": {"upc": ["0316714836010", "0316714835013"], "unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["0071a228-21cc-56a6-dcc9-a7a6ceea758c"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (16714-838-01)", "package_ndc": "16714-838-01", "marketing_start_date": "20180726"}], "brand_name": "ziprasidone", "product_id": "16714-838_cbe5f617-d390-54a0-2849-585abd37300f", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "16714-838", "generic_name": "ziprasidone", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA077565", "marketing_category": "ANDA", "marketing_start_date": "20180726", "listing_expiration_date": "20261231"}