NDC 85766-060 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC85766-060

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Sportpharm LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213967
Marketed since
August 12, 2020
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (8)

Package NDCDescriptionSince
85766-060-01100 TABLET, FILM COATED in 1 BOTTLE (85766-060-01)Aug 29, 2025
85766-060-05500 TABLET, FILM COATED in 1 BOTTLE (85766-060-05)Aug 29, 2025
85766-060-2121 TABLET, FILM COATED in 1 BOTTLE (85766-060-21)Apr 3, 2026
85766-060-2828 TABLET, FILM COATED in 1 BOTTLE (85766-060-28)Aug 29, 2025
85766-060-3030 TABLET, FILM COATED in 1 BOTTLE (85766-060-30)Aug 29, 2025
85766-060-4242 TABLET, FILM COATED in 1 BOTTLE (85766-060-42)Aug 29, 2025
85766-060-6060 TABLET, FILM COATED in 1 BOTTLE (85766-060-60)Aug 29, 2025
85766-060-9090 TABLET, FILM COATED in 1 BOTTLE (85766-060-90)Aug 29, 2025

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