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Methocarbamol

NDC 72789-041 · PD-Rx Pharmaceuticals, 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

72789-041-20 — 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-20)

72789-041-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-30)

72789-041-40 — 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-40)

72789-041-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72162-1929 — methocarbamol, 72162-1930 — methocarbamol, 72162-2487 — Methocarbamol, 72162-2488 — Methocarbamol, 72189-284 — METHOCARBAMOL, 72189-665 — Methocarbamol, 72245-873 — methocarbamol, 72789-012 — Methocarbamol, 72789-021 — Methocarbamol, 72789-022 — Methocarbamol, 72789-110 — Methocarbamol, 72789-397 — methocarbamol, 72789-398 — methocarbamol, 72789-428 — methocarbamol, 72789-429 — methocarbamol, 72789-481 — Methocarbamol, 72789-499 — Methocarbamol, 72789-521 — Methocarbamol, 72865-233 — Methocarbamol, 72865-234 — 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.