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Metoprolol Tartrate

NDC 42708-041 · QPharma Inc

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

Packages

42708-041-60 — 60 TABLET, FILM COATED in 1 BOTTLE (42708-041-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8422 — METOPROLOL, 0615-8423 — METOPROLOL, 25021-303 — Metoprolol Tartrate, 27241-301 — metoprolol tartrate and hydrochlorothiazide, 27241-302 — metoprolol tartrate and hydrochlorothiazide, 30698-458 — metoprolol tartrate, 30698-459 — metoprolol tartrate, 30698-460 — METOPROLOL TARTRATE, 30698-464 — Metoprolol Tartrate, 36000-033 — metoprolol tartrate, 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, +235 more

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