NDC 76420-670 – Diclofenac Sodium

Diclofenac Sodium 75 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC76420-670

Product details

Brand name
Diclofenac Sodium
Generic name
Diclofenac Sodium
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA077863
Marketed since
August 19, 2008
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 (6)

Package NDCDescriptionSince
76420-670-001000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-00)Mar 25, 2026
76420-670-01100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-01)Mar 7, 2024
76420-670-05500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-05)Mar 25, 2026
76420-670-3030 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-30)Mar 7, 2024
76420-670-6060 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-60)Mar 7, 2024
76420-670-9090 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-90)Mar 7, 2024

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