ziprasidone hydrochloride
Generic: ziprasidone hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
ziprasidone hydrochloride
Generic Name
ziprasidone hydrochloride
Labeler
remedyrepack inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
ziprasidone hydrochloride 80 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-1604
Product ID
70518-1604_494f01b2-8513-f5a5-e063-6294a90ab408
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077565
Listing Expiration
2027-12-31
Marketing Start
2018-10-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181604
Hyphenated Format
70518-1604
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 hydrochloride (source: ndc)
Generic Name
ziprasidone hydrochloride (source: ndc)
Application Number
ANDA077565 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mg/1
Packaging
- 30 CAPSULE in 1 BLISTER PACK (70518-1604-0)
- 30 POUCH in 1 BOX (70518-1604-1) / 1 CAPSULE in 1 POUCH (70518-1604-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "494f01b2-8513-f5a5-e063-6294a90ab408", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313778"], "spl_set_id": ["c8841b89-b451-4b7c-8110-6a3a58cb986a"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-1604-0)", "package_ndc": "70518-1604-0", "marketing_start_date": "20181026"}, {"sample": false, "description": "30 POUCH in 1 BOX (70518-1604-1) / 1 CAPSULE in 1 POUCH (70518-1604-2)", "package_ndc": "70518-1604-1", "marketing_start_date": "20190423"}], "brand_name": "ziprasidone hydrochloride", "product_id": "70518-1604_494f01b2-8513-f5a5-e063-6294a90ab408", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-1604", "generic_name": "ziprasidone hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA077565", "marketing_category": "ANDA", "marketing_start_date": "20181026", "listing_expiration_date": "20271231"}