Methocarbamol

NDC 60687-568 · American Health Packaging

Generic nameMethocarbamol

Dosage formTABLET

RouteORAL

Active ingredient(s)METHOCARBAMOL

Strength750 mg/1

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

Marketing categoryANDA

Packages

60687-568-01 — 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-568-01) / 1 TABLET in 1 BLISTER PACK (60687-568-11)

FDA lists these products with the same active ingredient.

51655-575 — Methocarbamol, 55150-223 — Methocarbamol, 55154-2129 — Methocarbamol, 55154-2130 — Methocarbamol, 55154-2334 — Methocarbamol, 55154-2335 — Methocarbamol, 55700-890 — methocarbamol, 59651-340 — Methocarbamol, 59651-341 — Methocarbamol, 60687-559 — Methocarbamol, 60760-592 — Methocarbamol Tablets, 60760-725 — methocarbamol, 60760-770 — Methocarbamol Tablets, 60760-875 — Methocarbamol, 61919-368 — METHOCARBAMOL, 61919-616 — Methocarbamol, 62207-754 — Methocarbamol Tablets, 62207-770 — Methocarbamol Tablets, 63187-019 — Methocarbamol, 63187-087 — Methocarbamol, +188 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.