NDC 68788-8784 – Diclofenac Sodium

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

Human Prescription Drug

Product NDC68788-8784

Product details

Brand name
Diclofenac Sodium
Generic name
Diclofenac Sodium
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090066
Marketed since
December 12, 2024
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 (5)

Package NDCDescriptionSince
68788-8784-1100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-1)Dec 12, 2024
68788-8784-330 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-3)Dec 12, 2024
68788-8784-660 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-6)Dec 12, 2024
68788-8784-8120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-8)Dec 12, 2024
68788-8784-990 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-9)Dec 12, 2024

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