NDC 80425-0020 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC80425-0020

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
July 2, 2018
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (3)

Package NDCDescriptionSince
80425-0020-130 TABLET, COATED in 1 BOTTLE (80425-0020-1)Jul 2, 2018
80425-0020-260 TABLET, COATED in 1 BOTTLE (80425-0020-2)Jul 2, 2018
80425-0020-390 TABLET, COATED in 1 BOTTLE (80425-0020-3)Jul 2, 2018

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