Diclofenac Sodium

Product NDC
43063-467
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA074514
Marketing category
ANDA
Substance
DICLOFENAC SODIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
43063-467-1414 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-467-14) 2013-08-23NoHistorical
43063-467-1515 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-467-15) 2013-08-23NoHistorical
43063-467-2020 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-467-20) 2013-08-23NoHistorical
43063-467-3030 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-467-30) 2013-08-23NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Diclofenac Sodium Delayed-Release Tablets, USP Rx only Prescribing InformationPD-Rx Pharmaceuticals, Inc.2026-03-18HUMAN PRESCRIPTION DRUG LABEL26