NDC 70771-1015 – Nateglinide

Nateglinide 60 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70771-1015

Product details

Brand name
Nateglinide
Generic name
Nateglinide
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205248
Marketed since
October 27, 2016
Listing expires
December 31, 2026
Pharmacologic class
Glinide

Active ingredients

Uses, dosage, side effects and warnings for Nateglinide →

Package NDC codes (6)

Package NDCDescriptionSince
70771-1015-01000 TABLET, FILM COATED in 1 BOTTLE (70771-1015-0)Oct 27, 2016
70771-1015-1100 TABLET, FILM COATED in 1 BOTTLE (70771-1015-1)Oct 27, 2016
70771-1015-330 TABLET, FILM COATED in 1 BOTTLE (70771-1015-3)Oct 27, 2016
70771-1015-410 BLISTER PACK in 1 CARTON (70771-1015-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1015-2)Oct 27, 2016
70771-1015-5500 TABLET, FILM COATED in 1 BOTTLE (70771-1015-5)Oct 27, 2016
70771-1015-990 TABLET, FILM COATED in 1 BOTTLE (70771-1015-9)Oct 27, 2016

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