NDC 72887-873 – methocarbamol

Methocarbamol 1000 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72887-873

Product details

Brand name
methocarbamol
Generic name
methocarbamol
Labeler
FH2 PHARMA LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212707
Marketed since
August 30, 2024
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (1)

Package NDCDescriptionSince
72887-873-0330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72887-873-03)Aug 30, 2024

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