NDC 71205-301 – Valsartan

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

Human Prescription Drug

Product NDC71205-301

Product details

Brand name
Valsartan
Generic name
Valsartan
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202696
Marketed since
September 19, 2016
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
71205-301-3030 TABLET, FILM COATED in 1 BOTTLE (71205-301-30)Aug 1, 2019
71205-301-6060 TABLET, FILM COATED in 1 BOTTLE (71205-301-60)Aug 1, 2019
71205-301-9090 TABLET, FILM COATED in 1 BOTTLE (71205-301-90)Aug 1, 2019

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