Methocarbamol

NDC 50090-1781 · A-S Medication Solutions

Generic nameMethocarbamol

Dosage formTABLET

RouteORAL

Active ingredient(s)METHOCARBAMOL

Strength750 mg/1

Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]

Marketing categoryANDA

Packages

50090-1781-0 20 TABLET in 1 BOTTLE (50090-1781-0)

50090-1781-1 40 TABLET in 1 BOTTLE (50090-1781-1)

50090-1781-2 28 TABLET in 1 BOTTLE (50090-1781-2)

50090-1781-3 30 TABLET in 1 BOTTLE (50090-1781-3)

50090-1781-4 60 TABLET in 1 BOTTLE (50090-1781-4)

50090-1781-6 100 TABLET in 1 BOTTLE (50090-1781-6)

50090-1781-7 12 TABLET in 1 BOTTLE (50090-1781-7)

FDA lists these products with the same active ingredient.

36000-302 — methocarbamol, 43063-903 — Methocarbamol Tablets, 43063-905 — Methocarbamol Tablets, 43547-226 — Methocarbamol, 43547-405 — Methocarbamol, 43598-839 — Methocarbamol, 45865-242 — Methocarbamol, 50090-0182 — Methocarbamol, 50090-0183 — Methocarbamol, 50090-0184 — Methocarbamol, 50090-1783 — Methocarbamol, 50090-3556 — Methocarbamol Tablets, 50090-3557 — Methocarbamol Tablets, 50090-3570 — Methocarbamol Tablets, 50090-3578 — Methocarbamol, 50090-3587 — Methocarbamol Tablets, 50090-3756 — Methocarbamol Tablets, 50090-4793 — Methocarbamol, 50090-5006 — methocarbamol, 50090-5008 — methocarbamol, +188 more

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