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 20 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1835
Product ID 70518-1835_4b33c442-08d0-369d-e063-6394a90a4cb6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077565
Listing Expiration 2027-12-31
Marketing Start 2019-01-30

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181835
Hyphenated Format 70518-1835

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 ANDA077565 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BLISTER PACK (70518-1835-0)
  • 30 POUCH in 1 BOX (70518-1835-1) / 1 CAPSULE in 1 POUCH (70518-1835-2)
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": "4b33c442-08d0-369d-e063-6394a90a4cb6", "openfda": {"unii": ["216X081ORU"], "rxcui": ["314286"], "spl_set_id": ["56370be6-42a2-4962-acdc-22b7c6e0e7fe"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-1835-0)", "package_ndc": "70518-1835-0", "marketing_start_date": "20190130"}, {"sample": false, "description": "30 POUCH in 1 BOX (70518-1835-1)  / 1 CAPSULE in 1 POUCH (70518-1835-2)", "package_ndc": "70518-1835-1", "marketing_start_date": "20191021"}], "brand_name": "ziprasidone hydrochloride", "product_id": "70518-1835_4b33c442-08d0-369d-e063-6394a90a4cb6", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-1835", "generic_name": "ziprasidone hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA077565", "marketing_category": "ANDA", "marketing_start_date": "20190130", "listing_expiration_date": "20271231"}