NDC 65862-671 – Repaglinide

Repaglinide 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC65862-671

Product details

Brand name
Repaglinide
Generic name
Repaglinide
Labeler
Aurobindo Pharma Limited
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 (3)

Package NDCDescriptionSince
65862-671-01100 TABLET in 1 BOTTLE (65862-671-01)Jan 22, 2014
65862-671-05500 TABLET in 1 BOTTLE (65862-671-05)Jan 22, 2014
65862-671-991000 TABLET in 1 BOTTLE (65862-671-99)Jan 22, 2014

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