NDC 71209-049 – Telmisartan

Telmisartan 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71209-049

Product details

Brand name
Telmisartan
Generic name
Telmisartan
Labeler
Cadila Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208605
Marketed since
February 5, 2015
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Telmisartan →

Package NDC codes (7)

Package NDCDescriptionSince
71209-049-0130 TABLET in 1 BOTTLE (71209-049-01)Dec 22, 2022
71209-049-0490 TABLET in 1 BOTTLE (71209-049-04)Dec 22, 2022
71209-049-05100 TABLET in 1 BOTTLE (71209-049-05)Dec 22, 2022
71209-049-10500 TABLET in 1 BOTTLE (71209-049-10)Dec 22, 2022
71209-049-111000 TABLET in 1 BOTTLE (71209-049-11)Dec 22, 2022
71209-049-1630 BLISTER PACK in 1 CARTON (71209-049-16) / 10 TABLET in 1 BLISTER PACKFeb 5, 2015
71209-049-1830 BLISTER PACK in 1 CARTON (71209-049-18) / 10 TABLET in 1 BLISTER PACKFeb 5, 2015

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