NDC 76420-572 – Diclofenac Sodium

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

Human Prescription Drug

Product NDC76420-572

Product details

Brand name
Diclofenac Sodium
Generic name
Diclofenac Sodium
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090066
Marketed since
December 31, 2010
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
76420-572-01100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-01)Mar 7, 2024
76420-572-3030 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-30)Mar 7, 2024
76420-572-6060 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-60)Mar 7, 2024
76420-572-9090 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-90)Mar 7, 2024

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