NDC 80425-0578 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC80425-0578

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
March 13, 2026
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (6)

Package NDCDescriptionSince
80425-0578-130 TABLET, COATED in 1 BOTTLE (80425-0578-1)Mar 13, 2026
80425-0578-260 TABLET, COATED in 1 BOTTLE (80425-0578-2)Mar 13, 2026
80425-0578-390 TABLET, COATED in 1 BOTTLE (80425-0578-3)Mar 13, 2026
80425-0578-4120 TABLET, COATED in 1 BOTTLE (80425-0578-4)Mar 13, 2026
80425-0578-5180 TABLET, COATED in 1 BOTTLE (80425-0578-5)Mar 13, 2026
80425-0578-612 TABLET, COATED in 1 BOTTLE (80425-0578-6)Mar 13, 2026

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