NDC 33342-058 – Irbesartan and Hydrochlorothiazide

Irbesartan 300 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC33342-058

Product details

Brand name
Irbesartan and Hydrochlorothiazide
Generic name
Irbesartan and Hydrochlorothiazide
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202414
Marketed since
September 27, 2012
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Irbesartan and Hydrochlorothiazide →

Package NDC codes (5)

Package NDCDescriptionSince
33342-058-063 BLISTER PACK in 1 CARTON (33342-058-06) / 10 TABLET, FILM COATED in 1 BLISTER PACKSep 27, 2012
33342-058-0730 TABLET, FILM COATED in 1 BOTTLE (33342-058-07)Sep 27, 2012
33342-058-1090 TABLET, FILM COATED in 1 BOTTLE (33342-058-10)Sep 27, 2012
33342-058-15500 TABLET, FILM COATED in 1 BOTTLE (33342-058-15)Sep 27, 2012
33342-058-399 BLISTER PACK in 1 CARTON (33342-058-39) / 10 TABLET, FILM COATED in 1 BLISTER PACKSep 27, 2012

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