NDC 70518-1723 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC70518-1723

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
December 10, 2018
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (7)

Package NDCDescriptionSince
70518-1723-230 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-2)Apr 16, 2019
70518-1723-330 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-3)May 12, 2022
70518-1723-430 TABLET, COATED in 1 BLISTER PACK (70518-1723-4)Oct 17, 2022
70518-1723-660 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-6)Dec 24, 2024
70518-1723-790 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-7)Jan 17, 2025
70518-1723-815 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-8)Mar 25, 2025
70518-1723-940 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-9)Oct 13, 2025

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