NDC 29300-235 – Valsartan

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

Human Prescription Drug

Product NDC29300-235

Product details

Brand name
Valsartan
Generic name
Valsartan
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209261
Marketed since
May 4, 2018
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
29300-235-101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-10)May 15, 2018
29300-235-1330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-13)May 15, 2018
29300-235-1990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-19)May 15, 2018

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