NDC 71335-2539 – Rosuvastatin

Rosuvastatin 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2539

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
71335-2539-130 TABLET, FILM COATED in 1 BOTTLE (71335-2539-1)Dec 10, 2024
71335-2539-290 TABLET, FILM COATED in 1 BOTTLE (71335-2539-2)Dec 10, 2024
71335-2539-360 TABLET, FILM COATED in 1 BOTTLE (71335-2539-3)Dec 10, 2024
71335-2539-4120 TABLET, FILM COATED in 1 BOTTLE (71335-2539-4)Dec 10, 2024
71335-2539-5180 TABLET, FILM COATED in 1 BOTTLE (71335-2539-5)Dec 10, 2024
71335-2539-6100 TABLET, FILM COATED in 1 BOTTLE (71335-2539-6)Dec 10, 2024

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