NDC 70518-0787-2 - Ziprasidone Hydrochloride

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
70518-0787
Requested NDC
70518-0787-2
Package NDCs from labels
70518-0787-0, 70518-0787-2, 70518-0787-1
Manufacturer
REMEDYREPACK INC.
Effective date
2026-07-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ziprasidone Hydrochloride - REMEDYREPACK INC.REMEDYREPACK INC.2026-07-15HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-0787-0Ziprasidone Hydrochloride30 in 1 BLISTER PACKCAPSULE3018
70518-0787-1Ziprasidone Hydrochloride30 in 1 BOXCAPSULE3018
70518-0787-2Ziprasidone Hydrochloride1 in 1 POUCHCAPSULE118

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-0787ZIPRASIDONE HYDROCHLORIDE CAPSULE [REMEDYREPACK INC.]13Current NDC, Legacy NDC, 3 package rows20250502_c9f8f635-cf3f-4c42-8bd1-45bbe19bf97e.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 110 of 110 · 2,182 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Renewal Firming Day Broad Spectrum SPF 30TITANIUM DIOXIDE, ZINC OXIDEBURT'S BEES, INC.18ceb5d8-4b76-6a54-e054-00144ff88e882015-06-18WarningsExact identifier
unii: 15FIX9V2JP
TiZO2TITANIUM DIOXIDE, ZINC OXIDEFallien Cosmeceuticals, LTD.30468afc-9616-4765-b046-12e97a0a78272010-12-20WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.