NDC 71335-1723 – Telmisartan

Telmisartan 80 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1723

Product details

Brand name
Telmisartan
Generic name
Telmisartan
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090032
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 Telmisartan →

Package NDC codes (3)

Package NDCDescriptionSince
71335-1723-190 TABLET in 1 BOTTLE (71335-1723-1)Apr 4, 2024
71335-1723-230 TABLET in 1 BOTTLE (71335-1723-2)Oct 20, 2020
71335-1723-3180 TABLET in 1 BOTTLE (71335-1723-3)Oct 20, 2020

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