NDC 59651-341 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC59651-341

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213967
Marketed since
August 12, 2020
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (2)

Package NDCDescriptionSince
59651-341-01100 TABLET, FILM COATED in 1 BOTTLE (59651-341-01)Aug 12, 2020
59651-341-05500 TABLET, FILM COATED in 1 BOTTLE (59651-341-05)Aug 12, 2020

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