NDC 71335-0970 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0970

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208507
Marketed since
January 15, 2018
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
71335-0970-015 TABLET, FILM COATED in 1 BOTTLE (71335-0970-0)Oct 18, 2018
71335-0970-114 TABLET, FILM COATED in 1 BOTTLE (71335-0970-1)Oct 18, 2018
71335-0970-230 TABLET, FILM COATED in 1 BOTTLE (71335-0970-2)Oct 18, 2018
71335-0970-320 TABLET, FILM COATED in 1 BOTTLE (71335-0970-3)Oct 18, 2018
71335-0970-460 TABLET, FILM COATED in 1 BOTTLE (71335-0970-4)Oct 18, 2018
71335-0970-5100 TABLET, FILM COATED in 1 BOTTLE (71335-0970-5)Oct 18, 2018
71335-0970-640 TABLET, FILM COATED in 1 BOTTLE (71335-0970-6)Oct 18, 2018
71335-0970-790 TABLET, FILM COATED in 1 BOTTLE (71335-0970-7)Oct 18, 2018
71335-0970-8120 TABLET, FILM COATED in 1 BOTTLE (71335-0970-8)Oct 18, 2018
71335-0970-97 TABLET, FILM COATED in 1 BOTTLE (71335-0970-9)Oct 18, 2018

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