NDC 60290-083 – Diclofenac Sodium

Diclofenac Sodium 50 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC60290-083

Product details

Brand name
Diclofenac Sodium
Generic name
Diclofenac Sodium
Labeler
Umedica Laboratories USA Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA219945
Marketed since
February 15, 2026
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Diclofenac Sodium →

Package NDC codes (4)

Package NDCDescriptionSince
60290-083-0160 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-083-01)Feb 15, 2026
60290-083-02100 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-083-02)Feb 15, 2026
60290-083-03500 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-083-03)Feb 15, 2026
60290-083-041000 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-083-04)Feb 15, 2026

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