NDC 42806-018 – Sulindac

Sulindac 150 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC42806-018

Product details

Brand name
Sulindac
Generic name
Sulindac
Labeler
Epic Pharma, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA072710
Marketed since
January 25, 2010
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Sulindac →

Package NDC codes (3)

Package NDCDescriptionSince
42806-018-01100 TABLET in 1 BOTTLE (42806-018-01)Jan 25, 2010
42806-018-05500 TABLET in 1 BOTTLE (42806-018-05)Jan 25, 2010
42806-018-101000 TABLET in 1 BOTTLE (42806-018-10)Jan 25, 2010

Recalls mentioning this NDC

Other Sulindac products