NDC 72789-041 – Methocarbamol

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

Human Prescription Drug

Product NDC72789-041

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208507
Marketed since
January 15, 2018
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (4)

Package NDCDescriptionSince
72789-041-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-20)Feb 13, 2020
72789-041-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-30)Jan 16, 2020
72789-041-4040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-40)Jan 6, 2020
72789-041-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-60)Dec 19, 2019

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