NDC 46708-459 – Amlodipine and Valsartan

Amlodipine Besylate 10 mg/1; Valsartan 160 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC46708-459

Product details

Brand name
Amlodipine and Valsartan
Generic name
Amlodipine and Valsartan
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202713
Marketed since
December 1, 2016
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Amlodipine And Valsartan →

Package NDC codes (5)

Package NDCDescriptionSince
46708-459-10100 TABLET, FILM COATED in 1 CARTON (46708-459-10)Dec 1, 2016
46708-459-3030 TABLET, FILM COATED in 1 BOTTLE (46708-459-30)Dec 1, 2016
46708-459-31100 TABLET, FILM COATED in 1 BOTTLE (46708-459-31)Dec 1, 2016
46708-459-71500 TABLET, FILM COATED in 1 BOTTLE (46708-459-71)Dec 1, 2016
46708-459-9090 TABLET, FILM COATED in 1 BOTTLE (46708-459-90)Dec 1, 2016

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