NDC 16571-201 – Diclofenac Sodium

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

Human Prescription Drug

Product NDC16571-201

Product details

Brand name
Diclofenac Sodium
Generic name
Diclofenac Sodium
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA077863
Marketed since
August 19, 2008
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
16571-201-0660 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (16571-201-06)Aug 19, 2008
16571-201-10100 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-10)Aug 19, 2008
16571-201-111000 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-11)Aug 19, 2008
16571-201-50500 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-50)Aug 19, 2008

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