Diclofenac Sodium

Product NDC
45865-436
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Medsource pharmaceuticals
Application
ANDA074514
Marketing category
ANDA
Substance
DICLOFENAC SODIUM
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
45865-436-3030 TABLET, DELAYED RELEASE in 1 BOTTLE (45865-436-30) 2018-12-120000-00-00NoCurrent
45865-436-6060 TABLET, DELAYED RELEASE in 1 BOTTLE (45865-436-60) 2018-12-120000-00-00NoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Diclofenac Sodium Delayed-Release Tablets, USP 40-9184 Revised – October 2017 Rx Only Prescribing InformationMedsource pharmaceuticals2019-12-29HUMAN PRESCRIPTION DRUG LABEL1