NDC 68788-8698 – Rosuvastatin

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

Human Prescription Drug

Product NDC68788-8698

Product details

Brand name
Rosuvastatin
Generic name
Rosuvastatin
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206381
Marketed since
June 14, 2024
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Rosuvastatin →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8698-220 TABLET, FILM COATED in 1 BOTTLE (68788-8698-2)Jun 14, 2024
68788-8698-330 TABLET, FILM COATED in 1 BOTTLE (68788-8698-3)Jun 14, 2024
68788-8698-660 TABLET, FILM COATED in 1 BOTTLE (68788-8698-6)Jun 14, 2024
68788-8698-990 TABLET, FILM COATED in 1 BOTTLE (68788-8698-9)Jun 14, 2024

Other Rosuvastatin products