ziprasidone

Generic: ziprasidone

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ziprasidone
Generic Name ziprasidone
Labeler major pharmaceuticals
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ziprasidone hydrochloride 40 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6270
Product ID 0904-6270_11aa05a7-d934-4932-990a-da13164d3825
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077565
Listing Expiration 2026-12-31
Marketing Start 2012-03-15

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046270
Hyphenated Format 0904-6270

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

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 40 BLISTER PACK in 1 CARTON (0904-6270-08) / 1 CAPSULE in 1 BLISTER PACK
  • 80 BLISTER PACK in 1 CARTON (0904-6270-45) / 1 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (2)

0904-6270-08 40 BLISTER PACK in 1 CARTON (0904-6270-08) / 1 CAPSULE in 1 BLISTER PACK 0904-6270-45 80 BLISTER PACK in 1 CARTON (0904-6270-45) / 1 CAPSULE in 1 BLISTER PACK

Ingredients (1)

ziprasidone hydrochloride (40 mg/1)

Linked Drug Pages (1)

Ziprasidone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "11aa05a7-d934-4932-990a-da13164d3825", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["ca55c149-5b9a-4144-b586-37cb5e84dc4e"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "40 BLISTER PACK in 1 CARTON (0904-6270-08)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6270-08", "marketing_start_date": "20120315"}, {"sample": false, "description": "80 BLISTER PACK in 1 CARTON (0904-6270-45)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6270-45", "marketing_start_date": "20120315"}], "brand_name": "Ziprasidone", "product_id": "0904-6270_11aa05a7-d934-4932-990a-da13164d3825", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0904-6270", "generic_name": "Ziprasidone", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA077565", "marketing_category": "ANDA", "marketing_start_date": "20120315", "listing_expiration_date": "20261231"}