ziprasidone
Generic: ziprasidone
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
ziprasidone
Generic Name
ziprasidone
Labeler
major pharmaceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
ziprasidone hydrochloride 80 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6272
Product ID
0904-6272_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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09046272
Hyphenated Format
0904-6272
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 80 mg/1
Packaging
- 40 BLISTER PACK in 1 CARTON (0904-6272-08) / 1 CAPSULE in 1 BLISTER PACK
- 80 BLISTER PACK in 1 CARTON (0904-6272-45) / 1 CAPSULE in 1 BLISTER PACK
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
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 (0904-6272-08) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6272-08", "marketing_start_date": "20120315"}, {"sample": false, "description": "80 BLISTER PACK in 1 CARTON (0904-6272-45) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6272-45", "marketing_start_date": "20120315"}], "brand_name": "Ziprasidone", "product_id": "0904-6272_11aa05a7-d934-4932-990a-da13164d3825", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0904-6272", "generic_name": "Ziprasidone", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA077565", "marketing_category": "ANDA", "marketing_start_date": "20120315", "listing_expiration_date": "20261231"}