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Methocarbamol Tablets, USP, 750 mg

NDC 63561-0174 · Granulation Technology, Inc.

Generic nameMethocarbamol
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)METHOCARBAMOL
Strength750 mg/1
Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Marketing categoryANDA

Packages

63561-0174-1 — 100 TABLET, FILM COATED in 1 BOTTLE (63561-0174-1)

63561-0174-5 — 500 TABLET, FILM COATED in 1 BOTTLE (63561-0174-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60760-875 — Methocarbamol, 61919-368 — METHOCARBAMOL, 61919-616 — Methocarbamol, 62207-754 — Methocarbamol Tablets, 62207-770 — Methocarbamol Tablets, 63187-019 — Methocarbamol, 63187-087 — Methocarbamol, 63187-130 — Methocarbamol, 63323-778 — Methocarbamol, 63561-0173 — Methocarbamol, 63629-1123 — Methocarbamol, 63629-1622 — Methocarbamol, 63629-2418 — methocarbamol, 63629-2419 — methocarbamol, 63629-2420 — methocarbamol, 63629-4882 — methocarbamol, 63629-8995 — Methocarbamol, 63629-9288 — methocarbamol, 66267-146 — Methocarbamol, 66267-803 — 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.