NDC 31722-534 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC31722-534

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090200
Marketed since
March 20, 2013
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (4)

Package NDCDescriptionSince
31722-534-0112 BOTTLE in 1 CASE (31722-534-01) / 100 TABLET in 1 BOTTLEMar 20, 2013
31722-534-0512 BOTTLE in 1 CASE (31722-534-05) / 500 TABLET in 1 BOTTLEMar 20, 2013
31722-534-3012 BOTTLE in 1 CASE (31722-534-30) / 30 TABLET in 1 BOTTLEMar 20, 2013
31722-534-6012 BOTTLE in 1 CASE (31722-534-60) / 60 TABLET in 1 BOTTLEMar 20, 2013

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