NDC 65862-572 – Valsartan

Valsartan 160 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 5 recalls

Product NDC65862-572

Product details

Brand name
Valsartan
Generic name
Valsartan
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202223
Marketed since
January 5, 2015
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Valsartan →

Package NDC codes (3)

Package NDCDescriptionSince
65862-572-1010 BLISTER PACK in 1 CARTON (65862-572-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKJan 5, 2015
65862-572-9090 TABLET, FILM COATED in 1 BOTTLE (65862-572-90)Jan 5, 2015
65862-572-991000 TABLET, FILM COATED in 1 BOTTLE (65862-572-99)Jan 5, 2015

Recalls mentioning this NDC

Other Valsartan products