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METOPROLOL TARTRATE

NDC 46708-291 · Alembic Pharmaceuticals Limited

Generic nameMETOPROLOL
Dosage formTABLET
RouteORAL
Active ingredient(s)METOPROLOL TARTRATE
Strength50 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

46708-291-10 — 100 TABLET in 1 CARTON (46708-291-10)

46708-291-30 — 30 TABLET in 1 BOTTLE (46708-291-30)

46708-291-31 — 100 TABLET in 1 BOTTLE (46708-291-31)

46708-291-91 — 1000 TABLET in 1 BOTTLE (46708-291-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42708-110 — Metoprolol Tartrate, 42708-147 — Metoprolol Tartrate, 42708-198 — METOPROLOL TARTRATE, 43063-821 — Metoprolol Tartrate, 43063-927 — Metoprolol Tartrate, 43063-938 — Metoprolol Tartrate, 46708-115 — Metoprolol Tartrate and Hydrochlorothiazide, 46708-116 — Metoprolol Tartrate and Hydrochlorothiazide, 46708-117 — Metoprolol Tartrate and Hydrochlorothiazide, 46708-290 — METOPROLOL, 46708-292 — METOPROLOL, 48433-073 — metoprolol tartrate, 48433-074 — metoprolol tartrate, 50090-1974 — Metoprolol Tartrate, 50090-1979 — Metoprolol Tartrate, 50090-2149 — Metoprolol Tartrate, 50090-2207 — Metoprolol Tartrate, 50090-2260 — Metoprolol Tartrate, 50090-5060 — Metoprolol Tartrate, 50090-5070 — Metoprolol Tartrate, +235 more

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