NDC 51660-143 – Valsartan

Valsartan 320 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51660-143

Product details

Brand name
Valsartan
Generic name
Valsartan
Labeler
Ohm Laboratories Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077492
Marketed since
July 7, 2014
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Valsartan →

Package NDC codes (3)

Package NDCDescriptionSince
51660-143-0310 TABLET, FILM COATED in 1 BOTTLE (51660-143-03)Jul 7, 2014
51660-143-05500 TABLET, FILM COATED in 1 BOTTLE (51660-143-05)Jul 7, 2014
51660-143-9090 TABLET, FILM COATED in 1 BOTTLE (51660-143-90)Jul 7, 2014

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