NDC 71335-1727 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1727

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA086988
Marketed since
January 15, 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
71335-1727-014 TABLET in 1 BOTTLE (71335-1727-0)Dec 29, 2021
71335-1727-120 TABLET in 1 BOTTLE (71335-1727-1)Apr 22, 2021
71335-1727-230 TABLET in 1 BOTTLE (71335-1727-2)Nov 5, 2020
71335-1727-340 TABLET in 1 BOTTLE (71335-1727-3)Feb 16, 2021
71335-1727-4120 TABLET in 1 BOTTLE (71335-1727-4)Apr 1, 2021
71335-1727-560 TABLET in 1 BOTTLE (71335-1727-5)Jan 8, 2021
71335-1727-690 TABLET in 1 BOTTLE (71335-1727-6)Nov 4, 2020
71335-1727-7112 TABLET in 1 BOTTLE (71335-1727-7)Dec 29, 2021
71335-1727-821 TABLET in 1 BOTTLE (71335-1727-8)Dec 29, 2021
71335-1727-984 TABLET in 1 BOTTLE (71335-1727-9)Dec 29, 2021

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