Diclofenac Sodium D/R

Product NDC
61919-075
11-digit product format
619190075
Labeler code
61919
Product ID
61919-075_c42fea0c-d812-061c-e053-2995a90a9b8d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium D/R
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Direct RX
Application
ANDA075185
Marketing category
ANDA
Marketing start
2014-01-01
Marketing end
0000-00-00
Substance
DICLOFENAC SODIUM
Active strength
75 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
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
61919-075-202021-01-29C16284748780-1ba0f9c33-5156-a910-e053-dadaa90a0b85Diclofenac Sodium D/R
61919-075-902021-01-29C16284748780-1ba0f9c33-3d1a-a910-e053-dadaa90a0b85Diclofenac Sodium D/R

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61919-075-30Diclofenac Sodium D/R30 in 1 BOTTLETABLET, DELAYED RELEASE3012
61919-075-60Diclofenac Sodium D/R60 in 1 BOTTLETABLET, DELAYED RELEASE6012
61919-075-20Diclofenac Sodium D/R20 in 1 BOTTLETABLET, DELAYED RELEASE201
61919-075-90Diclofenac Sodium D/R90 in 1 BOTTLETABLET, DELAYED RELEASE901

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
61919-075-20EA - Each61919-07583987e62-0c44-40f7-bf03-b1f8b1fd9bef12019-09-05
61919-075-30EA - Each61919-075d78b2402-79e2-45a8-aee9-32606811ae8e12014-05-02
61919-075-60EA - Each61919-075f958d846-9653-45ec-9757-88ba1ae78dd212015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DICLOFENAC SODIUMACTIVE INGREDIENTQTG126297QDICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
DICLOFENACACTIVE MOIETY144O8QL0L1DICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UDICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
FERROSOFERRIC OXIDEINACTIVE INGREDIENTXM0M87F357DICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WODICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XDICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30DICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)INACTIVE INGREDIENT74G4R6TH13DICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
POLYETHYLENE GLYCOL 2000INACTIVE INGREDIENTHAF0412YITDICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
POVIDONEINACTIVE INGREDIENTFZ989GH94EDICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
SHELLACINACTIVE INGREDIENT46N107B71ODICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2DICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
TALCINACTIVE INGREDIENT7SEV7J4R1UDICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPDICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61919-075DICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT RX]12Legacy NDC, 2 package rows20230408_2ae3c1e2-f053-4efb-9597-eeac4998d23f.zip
61919-075DICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT_RX]1Legacy NDC, 1 package rows20190817_903b77bf-6de1-2705-e053-2a95a90a0b93.zip
61919-075DICLOFENAC SODIUM D/R TABLET, DELAYED RELEASE [DIRECT_RX]1Legacy NDC, 1 package rows20190817_903b8d44-bfd7-718f-e053-2a95a90a712c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
855906diclofenac sodium 50 MG Delayed Release Oral TabletPSN2ae3c1e2-f053-4efb-9597-eeac4998d23f12
855926diclofenac sodium 75 MG Delayed Release Oral TabletPSN2ae3c1e2-f053-4efb-9597-eeac4998d23f12
855906diclofenac sodium 50 MG Delayed Release Oral TabletSCD2ae3c1e2-f053-4efb-9597-eeac4998d23f12
855926diclofenac sodium 75 MG Delayed Release Oral TabletSCD2ae3c1e2-f053-4efb-9597-eeac4998d23f12
855926diclofenac sodium 75 MG Delayed Release Oral TabletPSN903b77bf-6de1-2705-e053-2a95a90a0b931
855926diclofenac sodium 75 MG Delayed Release Oral TabletPSN903b8d44-bfd7-718f-e053-2a95a90a712c1
855926diclofenac sodium 75 MG Delayed Release Oral TabletSCD903b77bf-6de1-2705-e053-2a95a90a0b931
855926diclofenac sodium 75 MG Delayed Release Oral TabletSCD903b8d44-bfd7-718f-e053-2a95a90a712c1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
61919-075-206191900752020 in 1 BOTTLEHistorical
61919-075-306191900753030 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-075-30) 2014-01-010000-00-00NoNoCurrent
61919-075-606191900756060 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-075-60) 2014-01-010000-00-00NoNoCurrent
61919-075-906191900759090 in 1 BOTTLEHistorical