NDC 46708-755 – Amlodipine and Atorvastatin

Amlodipine Besylate 2.5 mg/1; Atorvastatin Calcium Trihydrate 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC46708-755

Product details

Brand name
Amlodipine and Atorvastatin
Generic name
Amlodipine and Atorvastatin
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217279
Marketed since
May 23, 2025
Listing expires
December 31, 2026
Pharmacologic class
Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker; HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Amlodipine and Atorvastatin →

Package NDC codes (2)

Package NDCDescriptionSince
46708-755-3030 TABLET, FILM COATED in 1 BOTTLE (46708-755-30)May 23, 2025
46708-755-9090 TABLET, FILM COATED in 1 BOTTLE (46708-755-90)May 23, 2025

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