NDC 51672-4052 – Etodolac

Etodolac 500 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC51672-4052

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
TaSun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076174
Marketed since
March 13, 2003
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Etodolac →

Package NDC codes (6)

Package NDCDescriptionSince
51672-4052-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4052-1)Mar 13, 2003
51672-4052-2500 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4052-2)Mar 13, 2003
51672-4052-31000 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4052-3)Mar 13, 2003
51672-4052-460 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4052-4)Mar 13, 2003
51672-4052-630 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4052-6)Mar 13, 2003
51672-4052-910 BLISTER PACK in 1 CARTON (51672-4052-9) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMar 13, 2003

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