NDC 70010-754 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC70010-754

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
Granules Pharmaceuticals Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
July 2, 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
70010-754-01100 TABLET, COATED in 1 BOTTLE (70010-754-01)Feb 1, 2020
70010-754-05500 TABLET, COATED in 1 BOTTLE (70010-754-05)Feb 1, 2020
70010-754-101000 TABLET, COATED in 1 BOTTLE (70010-754-10)Feb 1, 2020
70010-754-3524 TABLET, COATED in 1 BOTTLE (70010-754-35)Feb 1, 2020

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