ziprasidone

Generic: ziprasidone

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ziprasidone
Generic Name ziprasidone
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ziprasidone hydrochloride 60 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4475
Product ID 70518-4475_40d1f885-e7db-f6e4-e063-6294a90aeaef
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077565
Listing Expiration 2026-12-31
Marketing Start 2025-09-11

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184475
Hyphenated Format 70518-4475

Supplemental Identifiers

RxCUI
313777
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 (source: ndc)
Generic Name ziprasidone (source: ndc)
Application Number ANDA077565 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BLISTER PACK (70518-4475-0)
  • 30 POUCH in 1 BOX (70518-4475-1) / 1 CAPSULE in 1 POUCH (70518-4475-2)
source: ndc

Packages (2)

Ingredients (1)

ziprasidone hydrochloride (60 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40d1f885-e7db-f6e4-e063-6294a90aeaef", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313777"], "spl_set_id": ["48b54613-9b5f-4fcb-ba1f-22085ee0d8d1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4475-0)", "package_ndc": "70518-4475-0", "marketing_start_date": "20250911"}, {"sample": false, "description": "30 POUCH in 1 BOX (70518-4475-1)  / 1 CAPSULE in 1 POUCH (70518-4475-2)", "package_ndc": "70518-4475-1", "marketing_start_date": "20251010"}], "brand_name": "ziprasidone", "product_id": "70518-4475_40d1f885-e7db-f6e4-e063-6294a90aeaef", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4475", "generic_name": "ziprasidone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA077565", "marketing_category": "ANDA", "marketing_start_date": "20250911", "listing_expiration_date": "20261231"}