NDC 76420-258 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76420-258

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Asclemed USA, 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 (4)

Package NDCDescriptionSince
76420-258-10100 TABLET in 1 BOTTLE (76420-258-10)Aug 15, 2019
76420-258-3030 TABLET in 1 BOTTLE (76420-258-30)Aug 15, 2019
76420-258-6060 TABLET in 1 BOTTLE (76420-258-60)Aug 15, 2019
76420-258-9090 TABLET in 1 BOTTLE (76420-258-90)Aug 15, 2019

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