Skip to main content

METOPROLOL TARTRATE

NDC 0615-8422 · NCS HealthCare of KY, LLC dba Vangard Labs

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

0615-8422-05 — 15 TABLET in 1 BLISTER PACK (0615-8422-05)

0615-8422-39 — 30 TABLET in 1 BLISTER PACK (0615-8422-39)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0378-0032 — metoprolol tartrate, 0378-0047 — metoprolol tartrate, 0378-0424 — metoprolol tartrate and hydrochlorothiazide, 0378-0434 — metoprolol tartrate and hydrochlorothiazide, 0378-0445 — metoprolol tartrate and hydrochlorothiazide, 0378-4593 — metoprolol tartrate, 0378-4594 — metoprolol tartrate, 0409-1778 — METOPROLOL TARTRATE, 0409-2016 — METOPROLOL TARTRATE, 0615-8421 — 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, 42708-041 — 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.