NDC 71335-2406 – Rosuvastatin

Rosuvastatin 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2406

Product details

Brand name
Rosuvastatin
Generic name
Rosuvastatin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206381
Marketed since
April 24, 2019
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Rosuvastatin →

Package NDC codes (6)

Package NDCDescriptionSince
71335-2406-130 TABLET, FILM COATED in 1 BOTTLE (71335-2406-1)Jun 14, 2024
71335-2406-290 TABLET, FILM COATED in 1 BOTTLE (71335-2406-2)Jun 21, 2024
71335-2406-328 TABLET, FILM COATED in 1 BOTTLE (71335-2406-3)Nov 1, 2024
71335-2406-460 TABLET, FILM COATED in 1 BOTTLE (71335-2406-4)Nov 1, 2024
71335-2406-5180 TABLET, FILM COATED in 1 BOTTLE (71335-2406-5)Nov 1, 2024
71335-2406-6120 TABLET, FILM COATED in 1 BOTTLE (71335-2406-6)Nov 1, 2024

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