NDC 68071-3636 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3636

Product details

Brand name
Methocarbamol
Generic name
methocarbamol
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
August 15, 2019
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
68071-3636-66 TABLET in 1 BOTTLE (68071-3636-6)Jul 1, 2024

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