NDC 71335-2191 – Telmisartan

Telmisartan 80 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2191

Product details

Brand name
Telmisartan
Generic name
Telmisartan
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207882
Marketed since
August 20, 2017
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
71335-2191-190 TABLET in 1 BOTTLE (71335-2191-1)Dec 1, 2022
71335-2191-230 TABLET in 1 BOTTLE (71335-2191-2)Dec 1, 2022
71335-2191-3180 TABLET in 1 BOTTLE (71335-2191-3)Dec 1, 2022

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