NDC 71335-3105 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3105

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
May 22, 2025
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
71335-3105-160 TABLET in 1 BOTTLE (71335-3105-1)Mar 16, 2026
71335-3105-290 TABLET in 1 BOTTLE (71335-3105-2)Mar 16, 2026
71335-3105-330 TABLET in 1 BOTTLE (71335-3105-3)Mar 16, 2026
71335-3105-4120 TABLET in 1 BOTTLE (71335-3105-4)Mar 16, 2026
71335-3105-510 TABLET in 1 BOTTLE (71335-3105-5)Mar 16, 2026

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