NDC 87063-041 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC87063-041

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213967
Marketed since
August 12, 2020
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (6)

Package NDCDescriptionSince
87063-041-01100 TABLET, FILM COATED in 1 BOTTLE (87063-041-01)Nov 24, 2025
87063-041-1010 TABLET, FILM COATED in 1 BOTTLE (87063-041-10)Nov 24, 2025
87063-041-2020 TABLET, FILM COATED in 1 BOTTLE (87063-041-20)Nov 24, 2025
87063-041-3030 TABLET, FILM COATED in 1 BOTTLE (87063-041-30)Nov 24, 2025
87063-041-6060 TABLET, FILM COATED in 1 BOTTLE (87063-041-60)Nov 24, 2025
87063-041-9090 TABLET, FILM COATED in 1 BOTTLE (87063-041-90)Nov 24, 2025

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