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Methocarbamol

NDC 76420-040 · Asclemed USA, 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

76420-040-30 — 30 TABLET, FILM COATED in 1 BOTTLE (76420-040-30)

76420-040-60 — 60 TABLET, FILM COATED in 1 BOTTLE (76420-040-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72789-429 — methocarbamol, 72789-481 — Methocarbamol, 72789-499 — Methocarbamol, 72789-521 — Methocarbamol, 72865-233 — Methocarbamol, 72865-234 — Methocarbamol, 72887-873 — methocarbamol, 73352-510 — Methocarbamol, 76385-123 — Methocarbamol, 76385-124 — Methocarbamol, 76420-258 — methocarbamol, 76420-626 — methocarbamol, 76420-638 — methocarbamol, 76420-667 — methocarbamol, 76420-893 — Methocarbamol Tablets, 76420-894 — Methocarbamol Tablets, 80425-0020 — Methocarbamol, 80425-0021 — Methocarbamol, 80425-0138 — Methocarbamol, 80425-0171 — 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.