NDC 57237-159 – Repaglinide

Repaglinide 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC57237-159

Product details

Brand name
Repaglinide
Generic name
Repaglinide
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203820
Marketed since
January 22, 2014
Listing expires
December 31, 2026
Pharmacologic class
Glinide

Active ingredients

Uses, dosage, side effects and warnings for Repaglinide →

Package NDC codes (2)

Package NDCDescriptionSince
57237-159-01100 TABLET in 1 BOTTLE (57237-159-01)Jan 22, 2014
57237-159-05500 TABLET in 1 BOTTLE (57237-159-05)Jan 22, 2014

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