FDA.reportPublic FDA data

NDC 85509-1237-01 - CELECOXIB

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
85509-1237
Requested NDC
85509-1237-01
Package NDCs from labels
85509-1237-3, 85509-1237-6, 85509-1237-9, 85509-1237-1, 85509-1237-01
Manufacturer
PHOENIX RX LLC
Effective date
2025-08-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
CELECOXIB - PHOENIX RX LLCPHOENIX RX LLC2025-08-03HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85509-1237-1CELECOXIB120 in 1 BOTTLECAPSULE1202
85509-1237-3CELECOXIB30 in 1 BOTTLECAPSULE302
85509-1237-6CELECOXIB60 in 1 BOTTLECAPSULE602
85509-1237-9CELECOXIB90 in 1 BOTTLECAPSULE902

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
85509-1237-1EA - Each85509-1237f500da85-029b-4671-be10-46f27428585d12025-09-12
85509-1237-3EA - Each85509-1237d661fdef-264a-4bef-b32e-e37eb6ff3b6412025-09-12
85509-1237-6EA - Each85509-1237a22f33cc-44ad-456d-9ac0-a85dd4e0481212025-09-12
85509-1237-9EA - Each85509-12373e6cde98-a8a2-43d0-8ff0-37d7438d5a2812025-09-12

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 280 of 280 · 5,581 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.