NDC 80425-0577 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC80425-0577

Product details

Brand name
Methocarbamol
Generic name
methocarbamol
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
February 18, 2026
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (5)

Package NDCDescriptionSince
80425-0577-130 TABLET in 1 BOTTLE (80425-0577-1)Feb 18, 2026
80425-0577-260 TABLET in 1 BOTTLE (80425-0577-2)Feb 18, 2026
80425-0577-390 TABLET in 1 BOTTLE (80425-0577-3)Feb 18, 2026
80425-0577-4120 TABLET in 1 BOTTLE (80425-0577-4)Feb 18, 2026
80425-0577-5180 TABLET in 1 BOTTLE (80425-0577-5)Feb 18, 2026

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