NDC 68382-721 – Nateglinide

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

Human Prescription Drug

Product NDC68382-721

Product details

Brand name
Nateglinide
Generic name
Nateglinide
Labeler
Zydus Pharmaceuticals USA Inc.
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
68382-721-01100 TABLET, FILM COATED in 1 BOTTLE (68382-721-01)Oct 27, 2016
68382-721-05500 TABLET, FILM COATED in 1 BOTTLE (68382-721-05)Oct 27, 2016
68382-721-0630 TABLET, FILM COATED in 1 BOTTLE (68382-721-06)Oct 27, 2016
68382-721-101000 TABLET, FILM COATED in 1 BOTTLE (68382-721-10)Oct 27, 2016
68382-721-1690 TABLET, FILM COATED in 1 BOTTLE (68382-721-16)Oct 27, 2016
68382-721-7710 BLISTER PACK in 1 CARTON (68382-721-77) / 10 TABLET, FILM COATED in 1 BLISTER PACKOct 27, 2016

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