NDC 50090-3556 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC50090-3556

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
A-S Medication Solutions
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
July 2, 2018
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (7)

Package NDCDescriptionSince
50090-3556-020 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-0)Jul 2, 2018
50090-3556-140 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-1)Jul 2, 2018
50090-3556-228 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-2)Jul 2, 2018
50090-3556-330 TABLET, COATED in 1 BOTTLE (50090-3556-3)Aug 27, 2018
50090-3556-460 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-4)Jul 2, 2018
50090-3556-6100 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-6)Jul 2, 2018
50090-3556-712 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-7)Jul 2, 2018

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