NDC 68071-4520 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC68071-4520

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
July 2, 2018
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (4)

Package NDCDescriptionSince
68071-4520-220 TABLET, COATED in 1 BOTTLE (68071-4520-2)Aug 8, 2018
68071-4520-330 TABLET, COATED in 1 BOTTLE (68071-4520-3)Aug 8, 2018
68071-4520-660 TABLET, COATED in 1 BOTTLE (68071-4520-6)Jan 14, 2025
68071-4520-990 TABLET, COATED in 1 BOTTLE (68071-4520-9)Jan 30, 2026

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