NDC 71335-9669 – Rosuvastatin

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

Human Prescription Drug

Product NDC71335-9669

Product details

Brand name
Rosuvastatin
Generic name
Rosuvastatin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207616
Marketed since
October 29, 2016
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Rosuvastatin →

Package NDC codes (6)

Package NDCDescriptionSince
71335-9669-130 TABLET, FILM COATED in 1 BOTTLE (71335-9669-1)Apr 13, 2026
71335-9669-290 TABLET, FILM COATED in 1 BOTTLE (71335-9669-2)Apr 4, 2023
71335-9669-328 TABLET, FILM COATED in 1 BOTTLE (71335-9669-3)Apr 13, 2026
71335-9669-460 TABLET, FILM COATED in 1 BOTTLE (71335-9669-4)Apr 13, 2026
71335-9669-5180 TABLET, FILM COATED in 1 BOTTLE (71335-9669-5)Apr 13, 2026
71335-9669-6120 TABLET, FILM COATED in 1 BOTTLE (71335-9669-6)Apr 13, 2026

Other Rosuvastatin products