NDC 69584-612 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69584-612

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Oxford Pharmaceuticals, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
August 15, 2019
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
69584-612-0990 TABLET in 1 BOTTLE (69584-612-09)Aug 15, 2019
69584-612-10100 TABLET in 1 BOTTLE (69584-612-10)Aug 15, 2019
69584-612-50500 TABLET in 1 BOTTLE (69584-612-50)Aug 15, 2019
69584-612-901000 TABLET in 1 BOTTLE (69584-612-90)Aug 15, 2019

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