NDC 72789-481 – Methocarbamol Tablets, USP, 500 mg

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

Human Prescription Drug

Product NDC72789-481

Product details

Brand name
Methocarbamol Tablets, USP, 500 mg
Generic name
Methocarbamol
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212623
Marketed since
June 10, 2025
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol Tablets, USP, 500 mg →

Package NDC codes (7)

Package NDCDescriptionSince
72789-481-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-01)Jun 10, 2025
72789-481-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-30)Sep 3, 2025
72789-481-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-60)Jun 10, 2025
72789-481-82500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-82)Jun 10, 2025
72789-481-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-90)Jun 10, 2025
72789-481-93180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-93)Jun 10, 2025
72789-481-951000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-95)Jun 10, 2025

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