NDC 70868-910 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70868-910

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Key Therapeutics
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
January 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (1)

Package NDCDescriptionSince
70868-910-10100 TABLET in 1 BOTTLE (70868-910-10)Jan 1, 2021

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