NDC 82461-722 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC82461-722

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Medcore LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212623
Marketed since
July 31, 2026
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (1)

Package NDCDescriptionSince
82461-722-9090 TABLET, FILM COATED in 1 BOTTLE (82461-722-90)Jul 31, 2026

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