NDC 71335-0251 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0251

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090200
Marketed since
March 20, 2013
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0251-014 TABLET in 1 BOTTLE (71335-0251-0)Dec 27, 2021
71335-0251-120 TABLET in 1 BOTTLE (71335-0251-1)Mar 25, 2019
71335-0251-230 TABLET in 1 BOTTLE (71335-0251-2)Mar 12, 2018
71335-0251-340 TABLET in 1 BOTTLE (71335-0251-3)Mar 13, 2018
71335-0251-4120 TABLET in 1 BOTTLE (71335-0251-4)Feb 16, 2018
71335-0251-560 TABLET in 1 BOTTLE (71335-0251-5)Mar 7, 2018
71335-0251-690 TABLET in 1 BOTTLE (71335-0251-6)Mar 8, 2018
71335-0251-7112 TABLET in 1 BOTTLE (71335-0251-7)Dec 27, 2021
71335-0251-821 TABLET in 1 BOTTLE (71335-0251-8)Dec 27, 2021
71335-0251-984 TABLET in 1 BOTTLE (71335-0251-9)Dec 27, 2021

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