NDC 0480-3632 – Pitavastatin

Pitavastatin Calcium 2.09 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 2 recalls

Product NDC0480-3632

Product details

Brand name
Pitavastatin
Generic name
Pitavastatin calcium
Labeler
Teva Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205932
Marketed since
November 2, 2023
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pitavastatin →

Package NDC codes (1)

Package NDCDescriptionSince
0480-3632-9890 TABLET, FILM COATED in 1 BOTTLE (0480-3632-98)Nov 2, 2023

Recalls mentioning this NDC

Other Pitavastatin products