NDC 68788-8822 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8822

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090200
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 (7)

Package NDCDescriptionSince
68788-8822-1100 TABLET in 1 BOTTLE (68788-8822-1)Feb 10, 2025
68788-8822-220 TABLET in 1 BOTTLE (68788-8822-2)Feb 10, 2025
68788-8822-330 TABLET in 1 BOTTLE (68788-8822-3)Feb 10, 2025
68788-8822-440 TABLET in 1 BOTTLE (68788-8822-4)Feb 10, 2025
68788-8822-660 TABLET in 1 BOTTLE (68788-8822-6)Feb 10, 2025
68788-8822-8120 TABLET in 1 BOTTLE (68788-8822-8)Feb 10, 2025
68788-8822-990 TABLET in 1 BOTTLE (68788-8822-9)Feb 10, 2025

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