NDC 70868-901 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70868-901

Product details

Brand name
Methocarbamol
Generic name
methocarbamol
Labeler
Key Therapeutics
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
December 26, 2019
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
70868-901-9090 TABLET in 1 BOTTLE (70868-901-90)Dec 26, 2019

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