FDA.reportPublic FDA data

Diclofenac Sodium

Product NDC
50436-1003
11-digit product format
504361003
Labeler code
50436
Product ID
50436-1003_88f8011b-7072-4f65-8de8-ed9261a0298a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Unit Dose Services
Application
ANDA075185
Marketing category
ANDA
Marketing start
1998-11-13
Marketing end
0000-00-00
Substance
DICLOFENAC SODIUM
Active strength
75 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
111d457e-3138-4512-b0ba-d0cd760c4055Product name320250225
0426261e-1bb9-b78b-abd2-80da765a7e3eProduct name220240513
7b6158ae-c3f4-3d73-c35f-6f5d18b9efd7Product name520240320
0ac2f11f-f58d-baf2-71a0-680993b48a61Product name220231211
855d63c3-b090-4636-8fc7-6d39ad23c44fProduct name120230829
bb58f410-04be-65dd-9211-e89ead899698Product name620230323
0fcbc38a-8b29-3348-1cef-5222ea53484fProduct name420220516
c4e1eedc-aca2-4551-8382-89144ed9d049Product name320220126
8d368a34-1453-43ea-828d-0dbcd72b8794Product name820210622
d6bab9d2-edce-a213-4796-226ab15472c3Product name620200616
2487e6ef-d419-42fc-aaf8-7acc805d2370Product name220170718
e071c814-e5e7-e7ed-ec76-428765d9c66bProduct name220151120
93148e06-b8d7-4e6c-853e-62f807d17fbbProduct name120151014
dbb00be6-fb1c-4b0a-a770-31f7e05e247eProduct name120150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50436-1003-12024-01-30C16284748780-11030e365-115e-111a-e063-dadaa90a10e2Diclofenac Sodium
50436-1003-22024-01-30C16284748780-11030e365-115e-111a-e063-dadaa90a10e2Diclofenac Sodium

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50436-1003-1Diclofenac Sodium Delayed Release30 in 1 BOTTLETABLET, DELAYED RELEASE302
50436-1003-2Diclofenac Sodium Delayed Release60 in 1 BOTTLETABLET, DELAYED RELEASE602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50436-1003DICLOFENAC SODIUM DELAYED RELEASE (DICLOFENAC SODIUM) TABLET, DELAYED RELEASE [UNIT DOSE SERVICES]2Legacy NDC, 2 package rows20220513_f7ec92b6-1601-4f4e-87c8-531aae302f53.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
855926diclofenac sodium 75 MG Delayed Release Oral TabletPSNf7ec92b6-1601-4f4e-87c8-531aae302f532
855926diclofenac sodium 75 MG Delayed Release Oral TabletSCDf7ec92b6-1601-4f4e-87c8-531aae302f532

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50436-1003-15043610030130 TABLET, DELAYED RELEASE in 1 BOTTLE (50436-1003-1) 2022-04-010000-00-00NoNoCurrent
50436-1003-25043610030260 TABLET, DELAYED RELEASE in 1 BOTTLE (50436-1003-2) 2022-04-010000-00-00NoNoCurrent