NDC 68462-201 – Telmisartan

Telmisartan 80 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68462-201

Product details

Brand name
Telmisartan
Generic name
Telmisartan
Labeler
Glenmark Pharmaceuticals Inc., USA
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 (5)

Package NDCDescriptionSince
68462-201-01100 TABLET in 1 BOTTLE (68462-201-01)Jul 7, 2014
68462-201-133 BLISTER PACK in 1 CARTON (68462-201-13) / 10 TABLET in 1 BLISTER PACKJul 7, 2014
68462-201-3030 TABLET in 1 BOTTLE (68462-201-30)Dec 14, 2020
68462-201-784 BLISTER PACK in 1 CARTON (68462-201-78) / 10 TABLET in 1 BLISTER PACKDec 14, 2020
68462-201-9090 TABLET in 1 BOTTLE (68462-201-90)Mar 7, 2024

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