NDC 76420-667 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76420-667

Product details

Brand name
Methocarbamol
Generic name
methocarbamol
Labeler
Asclemed USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
January 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (4)

Package NDCDescriptionSince
76420-667-01100 TABLET in 1 BOTTLE (76420-667-01)Feb 8, 2024
76420-667-3030 TABLET in 1 BOTTLE (76420-667-30)Feb 8, 2024
76420-667-6060 TABLET in 1 BOTTLE (76420-667-60)Feb 8, 2024
76420-667-9090 TABLET in 1 BOTTLE (76420-667-90)Feb 8, 2024

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