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Methocarbamol

NDC 71205-103 · Proficient Rx LP

Generic nameMethocarbamol
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)METHOCARBAMOL
Strength500 mg/1
Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Marketing categoryANDA

Packages

71205-103-20 — 20 TABLET, FILM COATED in 1 BOTTLE (71205-103-20)

71205-103-30 — 30 TABLET, FILM COATED in 1 BOTTLE (71205-103-30)

71205-103-40 — 40 TABLET, FILM COATED in 1 BOTTLE (71205-103-40)

71205-103-45 — 45 TABLET, FILM COATED in 1 BOTTLE (71205-103-45)

71205-103-60 — 60 TABLET, FILM COATED in 1 BOTTLE (71205-103-60)

71205-103-90 — 90 TABLET, FILM COATED in 1 BOTTLE (71205-103-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 71205-068 — Methocarbamol Tablets, 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, 71335-1795 — 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.