NDC 73352-510 – Methocarbamol

Methocarbamol 1000 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC73352-510

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Trifluent Pharma LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA200958
Marketed since
February 10, 2025
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (1)

Package NDCDescriptionSince
73352-510-10100 TABLET, COATED in 1 BOTTLE (73352-510-10)Feb 10, 2025

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