NDC 59746-393 – Valsartan

Valsartan 320 mg/1 · Tablet · Oral

Human Prescription Drug 4 recalls

Product NDC59746-393

Product details

Brand name
Valsartan
Generic name
Valsartan
Labeler
Jubilant Cadista Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203536
Marketed since
August 24, 2026
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Valsartan →

Package NDC codes (4)

Package NDCDescriptionSince
59746-393-3030 TABLET in 1 BOTTLE (59746-393-30)Aug 24, 2026
59746-393-323 BLISTER PACK in 1 CARTON (59746-393-32) / 10 TABLET in 1 BLISTER PACKAug 24, 2026
59746-393-67400 TABLET in 1 BOTTLE (59746-393-67)Aug 24, 2026
59746-393-9090 TABLET in 1 BOTTLE (59746-393-90)Aug 24, 2026

Recalls mentioning this NDC

Other Valsartan products