NDC 71335-2383 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2383

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
August 15, 2019
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2383-015 TABLET in 1 BOTTLE (71335-2383-0)May 29, 2024
71335-2383-114 TABLET in 1 BOTTLE (71335-2383-1)May 29, 2024
71335-2383-230 TABLET in 1 BOTTLE (71335-2383-2)May 29, 2024
71335-2383-320 TABLET in 1 BOTTLE (71335-2383-3)May 29, 2024
71335-2383-460 TABLET in 1 BOTTLE (71335-2383-4)May 29, 2024
71335-2383-5100 TABLET in 1 BOTTLE (71335-2383-5)May 29, 2024
71335-2383-640 TABLET in 1 BOTTLE (71335-2383-6)May 29, 2024
71335-2383-790 TABLET in 1 BOTTLE (71335-2383-7)May 29, 2024
71335-2383-8120 TABLET in 1 BOTTLE (71335-2383-8)May 29, 2024
71335-2383-97 TABLET in 1 BOTTLE (71335-2383-9)May 29, 2024

Other Methocarbamol products