NDC 72865-309 – Simvastatin

Simvastatin 80 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72865-309

Product details

Brand name
Simvastatin
Generic name
Simvastatin
Labeler
XLCare Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200895
Marketed since
January 21, 2026
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Simvastatin →

Package NDC codes (6)

Package NDCDescriptionSince
72865-309-01100 TABLET, FILM COATED in 1 BOTTLE (72865-309-01)Jan 21, 2026
72865-309-05500 TABLET, FILM COATED in 1 BOTTLE (72865-309-05)Jan 21, 2026
72865-309-101000 TABLET, FILM COATED in 1 BOTTLE (72865-309-10)Jan 21, 2026
72865-309-3030 TABLET, FILM COATED in 1 BOTTLE (72865-309-30)Jan 21, 2026
72865-309-4545 TABLET, FILM COATED in 1 BOTTLE (72865-309-45)Jan 21, 2026
72865-309-9090 TABLET, FILM COATED in 1 BOTTLE (72865-309-90)Jan 21, 2026

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