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Methocarbamol

NDC 76420-667 · Asclemed USA, Inc.

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

Packages

76420-667-01 — 100 TABLET in 1 BOTTLE (76420-667-01)

76420-667-30 — 30 TABLET in 1 BOTTLE (76420-667-30)

76420-667-60 — 60 TABLET in 1 BOTTLE (76420-667-60)

76420-667-90 — 90 TABLET in 1 BOTTLE (76420-667-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72865-233 — Methocarbamol, 72865-234 — Methocarbamol, 72887-873 — methocarbamol, 73352-510 — Methocarbamol, 76385-123 — Methocarbamol, 76385-124 — Methocarbamol, 76420-040 — Methocarbamol, 76420-258 — methocarbamol, 76420-626 — methocarbamol, 76420-638 — methocarbamol, 76420-893 — Methocarbamol Tablets, 76420-894 — Methocarbamol Tablets, 80425-0020 — Methocarbamol, 80425-0021 — Methocarbamol, 80425-0138 — Methocarbamol, 80425-0171 — Methocarbamol, 80425-0275 — Methocarbamol, 80425-0283 — Methocarbamol, 80425-0490 — methocarbamol, 80425-0577 — 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.