Methocarbamol

NDC 70518-4501 · REMEDYREPACK INC.

Generic nameMethocarbamol Tablets

Dosage formTABLET, COATED

RouteORAL

Active ingredient(s)METHOCARBAMOL

Strength750 mg/1

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

Marketing categoryANDA

Packages

70518-4501-0 — 40 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4501-0)

FDA lists these products with the same active ingredient.

69528-701 — methocarbamol, 69584-611 — methocarbamol, 69584-612 — methocarbamol, 70010-754 — Methocarbamol Tablets, 70010-770 — Methocarbamol Tablets, 70069-101 — Methocarbamol, 70436-149 — methocarbamol, 70518-1723 — Methocarbamol Tablets, 70518-1738 — Methocarbamol Tablets, 70518-4472 — Methocarbamol, 70518-4603 — Methocarbamol Tablets, 70868-901 — methocarbamol, 70868-910 — methocarbamol, 71205-068 — Methocarbamol Tablets, 71205-103 — Methocarbamol, 71205-167 — Methocarbamol Tablets, 71205-285 — Methocarbamol, 71205-375 — Methocarbamol, 71288-716 — Methocarbamol, 71335-0251 — 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.