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Methocarbamol

NDC 68788-8867 · Preferred Pharmaceuticals Inc.

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

68788-8867-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68788-8867-3)

68788-8867-6 — 60 TABLET, FILM COATED in 1 BOTTLE (68788-8867-6)

68788-8867-9 — 90 TABLET, FILM COATED in 1 BOTTLE (68788-8867-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3636 — methocarbamol, 68071-3859 — Methocarbamol, 68071-4505 — Methocarbamol Tablets, 68071-4520 — Methocarbamol Tablets, 68083-317 — Methocarbamol, 68788-7973 — methocarbamol, 68788-7980 — methocarbamol, 68788-8172 — Methocarbamol Tablets, 68788-8213 — Methocarbamol Tablets, 68788-8822 — Methocarbamol, 68788-8876 — Methocarbamol, 68788-8880 — METHOCARBAMOL, 69306-500 — methocarbamol, 69306-510 — methocarbamol, 69528-701 — methocarbamol, 69584-611 — methocarbamol, 69584-612 — methocarbamol, 70010-754 — Methocarbamol Tablets, 70010-770 — Methocarbamol Tablets, 70069-101 — 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.