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
70518-1835
Product ID
70518-1835_4b33c442-08d0-369d-e063-6394a90a4cb6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077565
Listing Expiration
2027-12-31
Marketing Start
2019-01-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181835
Hyphenated Format
70518-1835
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
- 20 mg/1
Packaging
- 30 CAPSULE in 1 BLISTER PACK (70518-1835-0)
- 30 POUCH in 1 BOX (70518-1835-1) / 1 CAPSULE in 1 POUCH (70518-1835-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b33c442-08d0-369d-e063-6394a90a4cb6", "openfda": {"unii": ["216X081ORU"], "rxcui": ["314286"], "spl_set_id": ["56370be6-42a2-4962-acdc-22b7c6e0e7fe"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-1835-0)", "package_ndc": "70518-1835-0", "marketing_start_date": "20190130"}, {"sample": false, "description": "30 POUCH in 1 BOX (70518-1835-1) / 1 CAPSULE in 1 POUCH (70518-1835-2)", "package_ndc": "70518-1835-1", "marketing_start_date": "20191021"}], "brand_name": "ziprasidone hydrochloride", "product_id": "70518-1835_4b33c442-08d0-369d-e063-6394a90a4cb6", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-1835", "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": "ANDA077565", "marketing_category": "ANDA", "marketing_start_date": "20190130", "listing_expiration_date": "20271231"}