FDA.reportPublic FDA data

Diclofenac Sodium

Product NDC
50090-7881
11-digit product format
500907881
Labeler code
50090
Product ID
50090-7881_4b4436eb-d0eb-4026-9aad-bcb260deec96
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA075185
Marketing category
ANDA
Marketing start
2025-03-28
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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Diclofenac Sodium
Brand name suffix
Delayed Release
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DICLOFENAC SODIUM50 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiQTG126297Q
Rxcui855906

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
594e2c86-3079-4e6e-96c9-48f7a8afc78dProduct name120230718
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
50090-7881-0Diclofenac SodiumDelayed Release100 in 1 BOTTLETABLET, DELAYED RELEASE1001
50090-7881-2Diclofenac SodiumDelayed Release30 in 1 BOTTLETABLET, DELAYED RELEASE301
50090-7881-5Diclofenac SodiumDelayed Release90 in 1 BOTTLETABLET, DELAYED RELEASE901

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-7881-0EA - Each50090-78815b20bf36-a8b3-44af-9367-9455aa94e87d12026-03-17
50090-7881-2EA - Each50090-7881dec1587e-b347-409b-a1a4-59334ba3e2b812026-03-17
50090-7881-5EA - Each50090-78810d366a6d-c102-4811-969b-f750ebc149dd12026-03-17

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
855906diclofenac sodium 50 MG Delayed Release Oral TabletPSN0cefb675-c54e-44eb-b35c-38354b77eddd1
855906diclofenac sodium 50 MG Delayed Release Oral TabletSCD0cefb675-c54e-44eb-b35c-38354b77eddd1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
50090-7881-050090788100100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7881-0) 2026-02-04NoNoCurrent
50090-7881-25009078810230 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7881-2) 2026-02-04NoNoCurrent
50090-7881-55009078810590 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7881-5) 2026-02-04NoNoCurrent