NDC 51655-205 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC51655-205

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
January 8, 2023
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (2)

Package NDCDescriptionSince
51655-205-2020 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-205-20)Jan 8, 2023
51655-205-5230 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-205-52)Apr 13, 2023

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