NDC 43598-316 – Amlodipine besylate and Atorvastatin calcium

Amlodipine Besylate 5 mg/1; Atorvastatin Calcium Trihydrate 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 10 recalls

Product NDC43598-316

Product details

Brand name
Amlodipine besylate and Atorvastatin calcium
Generic name
Amlodipine besylate and Atorvastatin calcium
Labeler
Dr. Reddy's Laboratories Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203874
Marketed since
March 17, 2014
Listing expires
December 31, 2026
Pharmacologic class
Dihydropyridine Calcium Channel Blocker; HMG-CoA Reductase Inhibitor

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
43598-316-05500 TABLET, FILM COATED in 1 BOTTLE (43598-316-05)Mar 17, 2014
43598-316-3030 TABLET, FILM COATED in 1 BOTTLE (43598-316-30)Mar 17, 2014
43598-316-6060 TABLET, FILM COATED in 1 BOTTLE (43598-316-60)Mar 17, 2014
43598-316-9090 TABLET, FILM COATED in 1 BOTTLE (43598-316-90)Mar 17, 2014

Recalls mentioning this NDC

Other Amlodipine besylate and Atorvastatin calcium products