Methocarbamol

NDC 62207-754 · Granules India Ltd

Generic nameMethocarbamol Tablets

Dosage formTABLET, COATED

RouteORAL

Active ingredient(s)METHOCARBAMOL

Strength500 mg/1

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

Marketing categoryANDA

Packages

62207-754-41 — 24 TABLET, COATED in 1 BOTTLE (62207-754-41)

62207-754-43 — 100 TABLET, COATED in 1 BOTTLE (62207-754-43)

62207-754-47 — 500 TABLET, COATED in 1 BOTTLE (62207-754-47)

62207-754-49 — 1000 TABLET, COATED in 1 BOTTLE (62207-754-49)

FDA lists these products with the same active ingredient.

59651-340 — Methocarbamol, 59651-341 — Methocarbamol, 60687-559 — Methocarbamol, 60687-568 — Methocarbamol, 60760-592 — Methocarbamol Tablets, 60760-725 — methocarbamol, 60760-770 — Methocarbamol Tablets, 60760-875 — Methocarbamol, 61919-368 — METHOCARBAMOL, 61919-616 — Methocarbamol, 62207-770 — Methocarbamol Tablets, 63187-019 — Methocarbamol, 63187-087 — Methocarbamol, 63187-130 — Methocarbamol, 63323-778 — Methocarbamol, 63561-0173 — Methocarbamol, 63561-0174 — Methocarbamol, 63629-1123 — Methocarbamol, 63629-1622 — Methocarbamol, 63629-2418 — 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.