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 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-0743
Product ID
70518-0743_48338d61-a0c8-032e-e063-6294a90adf6d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204375
Listing Expiration
2027-12-31
Marketing Start
2017-09-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705180743
Hyphenated Format
70518-0743
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
ANDA204375 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 CAPSULE in 1 BLISTER PACK (70518-0743-0)
- 30 POUCH in 1 BOX (70518-0743-1) / 1 CAPSULE in 1 POUCH (70518-0743-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48338d61-a0c8-032e-e063-6294a90adf6d", "openfda": {"unii": ["216X081ORU"], "rxcui": ["314286"], "spl_set_id": ["4e7e2d5d-8ea8-4c25-a500-f4794542fda2"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-0743-0)", "package_ndc": "70518-0743-0", "marketing_start_date": "20170920"}, {"sample": false, "description": "30 POUCH in 1 BOX (70518-0743-1) / 1 CAPSULE in 1 POUCH (70518-0743-2)", "package_ndc": "70518-0743-1", "marketing_start_date": "20210804"}], "brand_name": "Ziprasidone Hydrochloride", "product_id": "70518-0743_48338d61-a0c8-032e-e063-6294a90adf6d", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-0743", "generic_name": "Ziprasidone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone Hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA204375", "marketing_category": "ANDA", "marketing_start_date": "20170920", "listing_expiration_date": "20271231"}