NDC 62332-088 – Telmisartan

Telmisartan 40 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC62332-088

Product details

Brand name
Telmisartan
Generic name
Telmisartan
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202130
Marketed since
June 25, 2016
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Telmisartan →

Package NDC codes (2)

Package NDCDescriptionSince
62332-088-3030 TABLET in 1 BOTTLE (62332-088-30)Jun 25, 2016
62332-088-911000 TABLET in 1 BOTTLE (62332-088-91)Jun 25, 2016

Recalls mentioning this NDC

Other Telmisartan products