NDC 70069-101 – Methocarbamol

Methocarbamol 100 mg/mL · Injection · Intramuscular, Intravenous

Human Prescription Drug 1 recall

Product NDC70069-101

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Somerset Therapeutics, LLC
Dosage form
Injection
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA207522
Marketed since
July 31, 2017
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (3)

Package NDCDescriptionSince
70069-101-055 VIAL in 1 CARTON (70069-101-05) / 10 mL in 1 VIALJul 31, 2017
70069-101-1010 VIAL in 1 CARTON (70069-101-10) / 10 mL in 1 VIALJul 31, 2017
70069-101-2525 VIAL in 1 CARTON (70069-101-25) / 10 mL in 1 VIALJul 31, 2017

Recalls mentioning this NDC

Other Methocarbamol products