NDC 51672-4051 – Etodolac

Etodolac 400 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC51672-4051

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
51672-4051-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4051-1)Mar 13, 2003
51672-4051-2500 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4051-2)Mar 13, 2003
51672-4051-31000 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4051-3)Mar 13, 2003
51672-4051-460 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4051-4)Mar 13, 2003
51672-4051-630 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4051-6)Mar 13, 2003
51672-4051-910 BLISTER PACK in 1 CARTON (51672-4051-9) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMar 13, 2003

Other Etodolac products