NDC 53489-479 – Sulindac

Sulindac 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC53489-479

Product details

Brand name
Sulindac
Generic name
Sulindac
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA072051
Marketed since
September 4, 2009
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Sulindac →

Package NDC codes (6)

Package NDCDescriptionSince
53489-479-01100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01)Sep 4, 2009
53489-479-0250 TABLET in 1 BOTTLE, PLASTIC (53489-479-02)Sep 4, 2009
53489-479-03250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03)Sep 4, 2009
53489-479-05500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05)Sep 4, 2009
53489-479-0660 TABLET in 1 BOTTLE, PLASTIC (53489-479-06)Sep 4, 2009
53489-479-101000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10)Sep 4, 2009

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