NDC 16571-759 – Nateglinide

Nateglinide 120 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC16571-759

Product details

Brand name
Nateglinide
Generic name
Nateglinide
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205544
Marketed since
December 16, 2020
Listing expires
December 31, 2026
Pharmacologic class
Glinide

Active ingredients

Uses, dosage, side effects and warnings for Nateglinide →

Package NDC codes (3)

Package NDCDescriptionSince
16571-759-01100 TABLET in 1 BOTTLE (16571-759-01)Dec 16, 2020
16571-759-0990 TABLET in 1 BOTTLE (16571-759-09)Dec 16, 2020
16571-759-50500 TABLET in 1 BOTTLE (16571-759-50)Dec 16, 2020

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