NDC 71335-0909 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71335-0909

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
Bryant Ranch Prepack
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 (10)

Package NDCDescriptionSince
71335-0909-014 TABLET, COATED in 1 BOTTLE (71335-0909-0)Aug 1, 2018
71335-0909-120 TABLET, COATED in 1 BOTTLE (71335-0909-1)Aug 6, 2018
71335-0909-230 TABLET, COATED in 1 BOTTLE (71335-0909-2)Aug 10, 2018
71335-0909-340 TABLET, COATED in 1 BOTTLE (71335-0909-3)Aug 28, 2018
71335-0909-4120 TABLET, COATED in 1 BOTTLE (71335-0909-4)Aug 8, 2018
71335-0909-560 TABLET, COATED in 1 BOTTLE (71335-0909-5)Jul 30, 2018
71335-0909-690 TABLET, COATED in 1 BOTTLE (71335-0909-6)Aug 1, 2018
71335-0909-7112 TABLET, COATED in 1 BOTTLE (71335-0909-7)Aug 1, 2018
71335-0909-821 TABLET, COATED in 1 BOTTLE (71335-0909-8)Aug 1, 2018
71335-0909-984 TABLET, COATED in 1 BOTTLE (71335-0909-9)Aug 1, 2018

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