NDC 72789-021 – Methocarbamol

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

Human Prescription Drug

Product NDC72789-021

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 (7)

Package NDCDescriptionSince
72789-021-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-01)Oct 24, 2019
72789-021-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-60)Sep 12, 2023
72789-021-82500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-82)Oct 24, 2019
72789-021-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-90)Sep 12, 2023
72789-021-93180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-93)Oct 24, 2019
72789-021-94270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-94)Oct 24, 2019
72789-021-99240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-99)Oct 24, 2019

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