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Methocarbamol

NDC 70518-1738 · REMEDYREPACK INC.

Generic nameMethocarbamol Tablets
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)METHOCARBAMOL
Strength750 mg/1
Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Marketing categoryANDA

Packages

70518-1738-4 — 30 TABLET, COATED in 1 BLISTER PACK (70518-1738-4)

70518-1738-6 — 60 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-6)

70518-1738-7 — 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-7)

70518-1738-8 — 30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-8)

70518-1738-9 — 15 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70436-149 — methocarbamol, 70518-1723 — Methocarbamol Tablets, 70518-4472 — Methocarbamol, 70518-4501 — Methocarbamol Tablets, 70518-4603 — Methocarbamol Tablets, 70868-901 — methocarbamol, 70868-910 — methocarbamol, 71205-068 — Methocarbamol Tablets, 71205-103 — Methocarbamol, 71205-167 — Methocarbamol Tablets, 71205-285 — Methocarbamol, 71205-375 — 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.