NDC 71205-167 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71205-167

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
Proficient Rx LP
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 (5)

Package NDCDescriptionSince
71205-167-066 TABLET, COATED in 1 BOTTLE (71205-167-06)May 13, 2026
71205-167-099 TABLET, COATED in 1 BOTTLE (71205-167-09)May 13, 2026
71205-167-3030 TABLET, COATED in 1 BOTTLE (71205-167-30)Dec 1, 2018
71205-167-6060 TABLET, COATED in 1 BOTTLE (71205-167-60)Dec 1, 2018
71205-167-9090 TABLET, COATED in 1 BOTTLE (71205-167-90)Dec 1, 2018

Other Methocarbamol products