Methocarbamol

NDC 71205-068 · Proficient Rx LP

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

71205-068-20 — 20 TABLET, COATED in 1 BOTTLE (71205-068-20)

71205-068-30 — 30 TABLET, COATED in 1 BOTTLE (71205-068-30)

71205-068-40 — 40 TABLET, COATED in 1 BOTTLE (71205-068-40)

71205-068-45 — 45 TABLET, COATED in 1 BOTTLE (71205-068-45)

71205-068-60 — 60 TABLET, COATED in 1 BOTTLE (71205-068-60)

71205-068-90 — 90 TABLET, COATED in 1 BOTTLE (71205-068-90)

FDA lists these products with the same active ingredient.

70010-770 — Methocarbamol Tablets, 70069-101 — Methocarbamol, 70436-149 — methocarbamol, 70518-1723 — Methocarbamol Tablets, 70518-1738 — Methocarbamol Tablets, 70518-4472 — Methocarbamol, 70518-4501 — Methocarbamol Tablets, 70518-4603 — Methocarbamol Tablets, 70868-901 — methocarbamol, 70868-910 — methocarbamol, 71205-103 — Methocarbamol, 71205-167 — Methocarbamol Tablets, 71205-285 — Methocarbamol, 71205-375 — Methocarbamol, 71288-716 — Methocarbamol, 71335-0251 — Methocarbamol, 71335-0828 — Methocarbamol, 71335-0909 — Methocarbamol Tablets, 71335-0970 — Methocarbamol, 71335-1727 — 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.