Diclofenac Sodium

Product NDC
50090-0538
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA074514
Marketing category
ANDA
Substance
DICLOFENAC SODIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-0538-0100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0538-0) 2014-11-28NoHistorical
50090-0538-230 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0538-2) 2016-06-29NoHistorical
50090-0538-590 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0538-5) 2016-06-29NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Diclofenac Sodium Delayed-Release Tablets, USP Rx only Prescribing InformationA-S Medication Solutions2026-01-15HUMAN PRESCRIPTION DRUG LABEL21