NDC 87063-135 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC87063-135

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
ASCLEMED USA INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
May 22, 2025
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (4)

Package NDCDescriptionSince
87063-135-01100 TABLET in 1 BOTTLE (87063-135-01)Mar 7, 2026
87063-135-3030 TABLET in 1 BOTTLE (87063-135-30)Mar 7, 2026
87063-135-6060 TABLET in 1 BOTTLE (87063-135-60)Mar 7, 2026
87063-135-9090 TABLET in 1 BOTTLE (87063-135-90)Mar 7, 2026

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