ziprasidone mesylate
Generic: ziprasidone mesylate
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
ziprasidone mesylate
Generic Name
ziprasidone mesylate
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
ziprasidone mesylate 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1564
Product ID
51662-1564_1035b793-4301-3cb4-e063-6294a90a5b1f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211908
Listing Expiration
2026-12-31
Marketing Start
2021-07-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621564
Hyphenated Format
51662-1564
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 mesylate (source: ndc)
Generic Name
ziprasidone mesylate (source: ndc)
Application Number
ANDA211908 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 10 POUCH in 1 CASE (51662-1564-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1564-2) / 5 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "1035b793-4301-3cb4-e063-6294a90a5b1f", "openfda": {"unii": ["3X6SAX83JZ"], "rxcui": ["351223"], "spl_set_id": ["c75971f8-9640-a6e8-e053-2995a90af654"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 POUCH in 1 CASE (51662-1564-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1564-2) / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1564-3", "marketing_start_date": "20210717"}], "brand_name": "ZIPRASIDONE MESYLATE", "product_id": "51662-1564_1035b793-4301-3cb4-e063-6294a90a5b1f", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "51662-1564", "generic_name": "ZIPRASIDONE MESYLATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZIPRASIDONE MESYLATE", "active_ingredients": [{"name": "ZIPRASIDONE MESYLATE", "strength": "20 mg/mL"}], "application_number": "ANDA211908", "marketing_category": "ANDA", "marketing_start_date": "20210717", "listing_expiration_date": "20261231"}