FDA.reportPublic FDA data

DICLOFENAC SODIUM

Product NDC
59651-842
11-digit product format
596510842
Labeler code
59651
Product ID
59651-842_3487033c-7c62-4034-8718-73a7c49b26a0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
DICLOFENAC SODIUM
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Aurobindo Pharma Limited
Application
ANDA075281
Marketing category
ANDA
Marketing start
2025-04-17
Substance
DICLOFENAC SODIUM
Active strength
50 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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
DICLOFENAC SODIUM
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DICLOFENAC SODIUM50 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiQTG126297Q
Rxcui855906, 855926

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59651-842-01DICLOFENAC SODIUM100 in 1 BOTTLETABLET, DELAYED RELEASE1001
59651-842-60DICLOFENAC SODIUM60 in 1 BOTTLETABLET, DELAYED RELEASE601
59651-842-99DICLOFENAC SODIUM1000 in 1 BOTTLETABLET, DELAYED RELEASE10001

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59651-842-01EA - Each59651-842eeae49b2-b86f-41a1-b0f8-a33ef907957412025-08-11
59651-842-60EA - Each59651-8427edd25f3-4828-49bb-91b2-7966c0052d6212025-08-11
59651-842-99EA - Each59651-842356ce01c-b2b0-440c-8640-30c75f11a6ed12025-08-11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59651-842DICLOFENAC SODIUM TABLET, DELAYED RELEASE [AUROBINDO PHARMA LIMITED]1Current NDC, 3 package rows20250510_3487033c-7c62-4034-8718-73a7c49b26a0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
855906diclofenac sodium 50 MG Delayed Release Oral TabletPSN3487033c-7c62-4034-8718-73a7c49b26a01
855906diclofenac sodium 50 MG Delayed Release Oral TabletPSN4dde6e36-7540-1cc3-e063-6294a90a39411
855926diclofenac sodium 75 MG Delayed Release Oral TabletPSN3487033c-7c62-4034-8718-73a7c49b26a01
855906diclofenac sodium 50 MG Delayed Release Oral TabletSCD3487033c-7c62-4034-8718-73a7c49b26a01
855906diclofenac sodium 50 MG Delayed Release Oral TabletSCD4dde6e36-7540-1cc3-e063-6294a90a39411
855926diclofenac sodium 75 MG Delayed Release Oral TabletSCD3487033c-7c62-4034-8718-73a7c49b26a01

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
59651-842-0159651084201100 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-842-01) 2025-04-17NoNoCurrent
59651-842-605965108426060 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-842-60) 2025-04-17NoNoCurrent
59651-842-99596510842991000 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-842-99) 2025-04-17NoNoCurrent