NDC 0615-8507 – Methocarbamol

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

Human Prescription Drug

Product NDC0615-8507

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
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 (1)

Package NDCDescriptionSince
0615-8507-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8507-39)Mar 12, 2024

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