ziprasidone hydrochloride

Generic: ziprasidone hydrochloride

Labeler: mckesson corporation dba sky packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ziprasidone hydrochloride
Generic Name ziprasidone hydrochloride
Labeler mckesson corporation dba sky packaging
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ziprasidone hydrochloride 40 mg/1

Manufacturer
McKesson Corporation dba SKY Packaging

Identifiers & Regulatory

Product NDC 63739-005
Product ID 63739-005_2b9c7a48-1373-ab1f-e063-6294a90a5e94
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077565
Marketing Start 2012-03-02
Marketing End 2026-03-31

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63739005
Hyphenated Format 63739-005

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 hydrochloride (source: ndc)
Application Number ANDA077565 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 4 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-005-32) / 10 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (1)

63739-005-32 4 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-005-32) / 10 CAPSULE in 1 BLISTER PACK

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": "2b9c7a48-1373-ab1f-e063-6294a90a5e94", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["db621e08-aa2a-43b9-9d6e-33a633c0f648"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-005-32)  / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "63739-005-32", "marketing_end_date": "20260331", "marketing_start_date": "20160111"}], "brand_name": "ziprasidone hydrochloride", "product_id": "63739-005_2b9c7a48-1373-ab1f-e063-6294a90a5e94", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "63739-005", "generic_name": "ziprasidone hydrochloride", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA077565", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20120302"}