NDC 66267-146 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC66267-146

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
NuCare 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 (6)

Package NDCDescriptionSince
66267-146-1212 TABLET in 1 BOTTLE (66267-146-12)Oct 10, 2016
66267-146-2020 TABLET in 1 BOTTLE (66267-146-20)Oct 10, 2016
66267-146-3030 TABLET in 1 BOTTLE (66267-146-30)Oct 10, 2016
66267-146-4040 TABLET in 1 BOTTLE (66267-146-40)Oct 10, 2016
66267-146-6060 TABLET in 1 BOTTLE (66267-146-60)Oct 10, 2016
66267-146-9090 TABLET in 1 BOTTLE (66267-146-90)Oct 10, 2016

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