NDC 71205-103 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71205-103

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208507
Marketed since
January 15, 2018
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (6)

Package NDCDescriptionSince
71205-103-2020 TABLET, FILM COATED in 1 BOTTLE (71205-103-20)Sep 4, 2018
71205-103-3030 TABLET, FILM COATED in 1 BOTTLE (71205-103-30)Sep 4, 2018
71205-103-4040 TABLET, FILM COATED in 1 BOTTLE (71205-103-40)Sep 4, 2018
71205-103-4545 TABLET, FILM COATED in 1 BOTTLE (71205-103-45)Sep 4, 2018
71205-103-6060 TABLET, FILM COATED in 1 BOTTLE (71205-103-60)Sep 4, 2018
71205-103-9090 TABLET, FILM COATED in 1 BOTTLE (71205-103-90)Sep 4, 2018

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