NDC 70518-1738 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC70518-1738

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 17, 2018
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (5)

Package NDCDescriptionSince
70518-1738-430 TABLET, COATED in 1 BLISTER PACK (70518-1738-4)Apr 29, 2022
70518-1738-660 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-6)Jun 22, 2023
70518-1738-790 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-7)Aug 16, 2022
70518-1738-830 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-8)Jan 11, 2023
70518-1738-915 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-9)Mar 31, 2025

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