NDC 70518-4603 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC70518-4603

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
April 22, 2026
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (3)

Package NDCDescriptionSince
70518-4603-040 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4603-0)Apr 22, 2026
70518-4603-150 POUCH in 1 BOX (70518-4603-1) / 1 TABLET, COATED in 1 POUCH (70518-4603-2)Apr 27, 2026
70518-4603-3100 POUCH in 1 BOX (70518-4603-3) / 1 TABLET, COATED in 1 POUCH (70518-4603-4)Aug 10, 2026

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