NDC 71335-2305 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2305

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
71335-2305-014 TABLET in 1 BOTTLE (71335-2305-0)Apr 3, 2024
71335-2305-120 TABLET in 1 BOTTLE (71335-2305-1)Apr 3, 2024
71335-2305-230 TABLET in 1 BOTTLE (71335-2305-2)Dec 15, 2023
71335-2305-340 TABLET in 1 BOTTLE (71335-2305-3)Apr 3, 2024
71335-2305-4120 TABLET in 1 BOTTLE (71335-2305-4)Nov 27, 2023
71335-2305-560 TABLET in 1 BOTTLE (71335-2305-5)Dec 28, 2023
71335-2305-690 TABLET in 1 BOTTLE (71335-2305-6)Nov 16, 2023
71335-2305-7112 TABLET in 1 BOTTLE (71335-2305-7)Apr 3, 2024
71335-2305-821 TABLET in 1 BOTTLE (71335-2305-8)Apr 3, 2024
71335-2305-984 TABLET in 1 BOTTLE (71335-2305-9)Apr 3, 2024

Other Methocarbamol products