NDC 60760-874 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC60760-874

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
St. Mary's Medical Park Pharmacy
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213967
Marketed since
September 17, 2026
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (1)

Package NDCDescriptionSince
60760-874-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-874-90)Sep 17, 2026

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