ziprasidone hydrochloride

Generic: ziprasidone hcl

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ziprasidone hydrochloride
Generic Name ziprasidone hcl
Labeler american health packaging
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ziprasidone hydrochloride 20 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-103
Product ID 68084-103_3d34b9a4-f85e-f66c-e063-6394a90a0518
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077561
Listing Expiration 2026-12-31
Marketing Start 2014-12-16

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68084103
Hyphenated Format 68084-103

Supplemental Identifiers

RxCUI
313776 313777 313778 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 hcl (source: ndc)
Application Number ANDA077561 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 80 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-103-09) / 1 CAPSULE in 1 BLISTER PACK (68084-103-11)
source: ndc

Packages (1)

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": "3d34b9a4-f85e-f66c-e063-6394a90a0518", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["ba039e48-7bde-4fc5-bd39-8c9dfa98fada"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "80 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-103-09)  / 1 CAPSULE in 1 BLISTER PACK (68084-103-11)", "package_ndc": "68084-103-09", "marketing_start_date": "20141216"}], "brand_name": "Ziprasidone Hydrochloride", "product_id": "68084-103_3d34b9a4-f85e-f66c-e063-6394a90a0518", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68084-103", "generic_name": "Ziprasidone HCl", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone Hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA077561", "marketing_category": "ANDA", "marketing_start_date": "20141216", "listing_expiration_date": "20261231"}