NDC 0093-7443 – Fluvastatin

Fluvastatin Sodium 40 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC0093-7443

Product details

Brand name
Fluvastatin
Generic name
Fluvastatin
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078407
Marketed since
July 5, 2012
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluvastatin →

Package NDC codes (2)

Package NDCDescriptionSince
0093-7443-01100 CAPSULE in 1 BOTTLE (0093-7443-01)Jul 10, 2012
0093-7443-5630 CAPSULE in 1 BOTTLE (0093-7443-56)Jul 5, 2012

Recalls mentioning this NDC

Other Fluvastatin products