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Metoprolol Tartrate and Hydrochlorothiazide

NDC 46708-117 · Alembic Pharmaceuticals Limited

Generic nameMetoprolol Tartrate and Hydrochlorothiazide
Dosage formTABLET
RouteORAL
Active ingredient(s)METOPROLOL TARTRATE, HYDROCHLOROTHIAZIDE
Strength50; 100 mg/1; mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

46708-117-10 — 100 TABLET in 1 BOTTLE (46708-117-10)

46708-117-30 — 30 TABLET in 1 BOTTLE (46708-117-30)

46708-117-50 — 500 TABLET in 1 BOTTLE (46708-117-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43547-424 — losartan potassium and hydrochlorothiazide, 43547-425 — losartan potassium and hydrochlorothiazide, 43547-441 — telmisartan and hydrochlorothiazide, 43547-442 — telmisartan and hydrochlorothiazide, 43547-443 — telmisartan and hydrochlorothiazide, 43547-459 — candesartan cilexetil and hydrochlorothiazide, 43547-460 — candesartan cilexetil and hydrochlorothiazide, 43547-461 — candesartan cilexetil and hydrochlorothiazide, 46708-115 — Metoprolol Tartrate and Hydrochlorothiazide, 46708-116 — Metoprolol Tartrate and Hydrochlorothiazide, 46708-149 — Olmesartan Medoxomil and Hydrochlorothiazide, 46708-150 — Olmesartan Medoxomil and Hydrochlorothiazide, 46708-151 — Olmesartan Medoxomil and Hydrochlorothiazide, 46708-209 — Telmisartan and Hydrochlorothiazide, 46708-210 — Telmisartan and Hydrochlorothiazide, 46708-211 — Telmisartan and Hydrochlorothiazide, 46708-290 — METOPROLOL, 46708-291 — METOPROLOL, 46708-292 — METOPROLOL, 46708-438 — Hydrochlorothiazide, +1096 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.