NDC 80425-0579 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC80425-0579

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 25, 2025
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
80425-0579-130 TABLET, COATED in 1 BOTTLE (80425-0579-1)Mar 25, 2025
80425-0579-260 TABLET, COATED in 1 BOTTLE (80425-0579-2)Mar 25, 2025
80425-0579-390 TABLET, COATED in 1 BOTTLE (80425-0579-3)Mar 25, 2025
80425-0579-4120 TABLET, COATED in 1 BOTTLE (80425-0579-4)Mar 25, 2025
80425-0579-5180 TABLET, COATED in 1 BOTTLE (80425-0579-5)Mar 25, 2025
80425-0579-612 TABLET, COATED in 1 BOTTLE (80425-0579-6)Mar 25, 2025

Other Methocarbamol products