NDC 76420-893 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC76420-893

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
July 2, 2018
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (6)

Package NDCDescriptionSince
76420-893-01100 TABLET, COATED in 1 BOTTLE (76420-893-01)Jan 28, 2025
76420-893-05500 TABLET, COATED in 1 BOTTLE (76420-893-05)Jan 28, 2025
76420-893-12120 TABLET, COATED in 1 BOTTLE (76420-893-12)Jan 28, 2025
76420-893-3030 TABLET, COATED in 1 BOTTLE (76420-893-30)Jan 28, 2025
76420-893-6060 TABLET, COATED in 1 BOTTLE (76420-893-60)Jan 28, 2025
76420-893-9090 TABLET, COATED in 1 BOTTLE (76420-893-90)Jan 28, 2025

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