ziprasidone hydrochloride

Generic: ziprasidone hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ziprasidone hydrochloride
Generic Name ziprasidone hydrochloride
Labeler proficient rx lp
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ziprasidone hydrochloride 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-168
Product ID 63187-168_67b8d9a0-2da1-4a8d-8775-ecbe065870d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077562
Listing Expiration 2026-12-31
Marketing Start 2013-02-13

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187168
Hyphenated Format 63187-168

Supplemental Identifiers

RxCUI
314286
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 ANDA077562 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (63187-168-30)
  • 60 CAPSULE in 1 BOTTLE (63187-168-60)
source: ndc

Packages (2)

Ingredients (1)

ziprasidone hydrochloride (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "67b8d9a0-2da1-4a8d-8775-ecbe065870d4", "openfda": {"unii": ["216X081ORU"], "rxcui": ["314286"], "spl_set_id": ["b650e8b6-6df7-4301-837d-3d3b650b7456"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (63187-168-30)", "package_ndc": "63187-168-30", "marketing_start_date": "20190101"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (63187-168-60)", "package_ndc": "63187-168-60", "marketing_start_date": "20190101"}], "brand_name": "ziprasidone hydrochloride", "product_id": "63187-168_67b8d9a0-2da1-4a8d-8775-ecbe065870d4", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "63187-168", "generic_name": "ziprasidone hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA077562", "marketing_category": "ANDA", "marketing_start_date": "20130213", "listing_expiration_date": "20261231"}