Diclofenac Sodium

Product NDC
50090-6924
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077863
Marketing category
ANDA
Substance
DICLOFENAC SODIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6924-090 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-6924-0) 2023-12-14NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Diclofenac Sodium Delayed-release Tablets, USP 25 mg, 50 mg and 75 mgA-S Medication Solutions2023-12-25Human Prescription Drug Label1