NDC 68382-472 – Telmisartan

Telmisartan 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-472

Product details

Brand name
Telmisartan
Generic name
Telmisartan
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203325
Marketed since
August 27, 2014
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Telmisartan →

Package NDC codes (6)

Package NDCDescriptionSince
68382-472-01100 TABLET in 1 BOTTLE (68382-472-01)Aug 27, 2014
68382-472-05500 TABLET in 1 BOTTLE (68382-472-05)Aug 27, 2014
68382-472-0630 TABLET in 1 BOTTLE (68382-472-06)Aug 27, 2014
68382-472-101000 TABLET in 1 BOTTLE (68382-472-10)Aug 27, 2014
68382-472-1690 TABLET in 1 BOTTLE (68382-472-16)Aug 27, 2014
68382-472-7830 BLISTER PACK in 1 CARTON (68382-472-78) / 1 TABLET in 1 BLISTER PACK (68382-472-30)Aug 27, 2014

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