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Methocarbamol

NDC 80425-0138 · Advanced Rx Pharmacy of Tennessee, LLC

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

80425-0138-1 — 60 TABLET, FILM COATED in 1 BOTTLE (80425-0138-1)

80425-0138-2 — 90 TABLET, FILM COATED in 1 BOTTLE (80425-0138-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76385-124 — Methocarbamol, 76420-040 — 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, 80425-0171 — Methocarbamol, 80425-0275 — Methocarbamol, 80425-0283 — Methocarbamol, 80425-0490 — methocarbamol, 80425-0577 — methocarbamol, 80425-0578 — Methocarbamol Tablets, 80425-0579 — Methocarbamol Tablets, 82461-722 — Methocarbamol, 82461-723 — Methocarbamol, 82804-121 — 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.