FDA.reportPublic FDA data

NDC 70518-0993-2 - PAROXETINE

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
70518-0993
Requested NDC
70518-0993-2
Package NDCs from labels
70518-0993-0, 70518-0993-2, 70518-0993-1
Manufacturer
REMEDYREPACK INC.
Effective date
2026-09-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PAROXETINE - REMEDYREPACK INC.REMEDYREPACK INC.2026-09-24HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-0993-0PAROXETINE30 in 1 BLISTER PACKTABLET, FILM COATED3017
70518-0993-1PAROXETINE100 in 1 BOXTABLET, FILM COATED10017
70518-0993-2PAROXETINE1 in 1 POUCHTABLET, FILM COATED117

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-0993PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [REMEDYREPACK INC.]14Current NDC, Legacy NDC, 3 package rows20250424_beb87e2e-0a8f-43b6-b148-57f0b7191548.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 103 of 103 · 2,041 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
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.