ziprasidone hydrochloride

Generic: ziprasidone hydrochloride

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

Drug Facts

Product Profile

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

ziprasidone hydrochloride 40 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-0787
Product ID 70518-0787_4b312260-703f-713e-e063-6294a90a17f2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204375
Listing Expiration 2027-12-31
Marketing Start 2017-10-13

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705180787
Hyphenated Format 70518-0787

Supplemental Identifiers

RxCUI
313776
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 ANDA204375 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 POUCH in 1 BOX (70518-0787-1) / 1 CAPSULE in 1 POUCH (70518-0787-2)
source: ndc

Packages (1)

70518-0787-1 30 POUCH in 1 BOX (70518-0787-1) / 1 CAPSULE in 1 POUCH (70518-0787-2)

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": "4b312260-703f-713e-e063-6294a90a17f2", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313776"], "spl_set_id": ["c9f8f635-cf3f-4c42-8bd1-45bbe19bf97e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-0787-1)  / 1 CAPSULE in 1 POUCH (70518-0787-2)", "package_ndc": "70518-0787-1", "marketing_start_date": "20210728"}], "brand_name": "Ziprasidone Hydrochloride", "product_id": "70518-0787_4b312260-703f-713e-e063-6294a90a17f2", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-0787", "generic_name": "Ziprasidone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone Hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA204375", "marketing_category": "ANDA", "marketing_start_date": "20171013", "listing_expiration_date": "20271231"}