NDC 35561-212 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC35561-212

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Bostal LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA200958
Marketed since
October 10, 2018
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
35561-212-12100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-12)Oct 10, 2018
35561-212-13500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-13)Oct 10, 2018

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