NDC 71205-285 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71205-285

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 (5)

Package NDCDescriptionSince
71205-285-3030 TABLET, FILM COATED in 1 BOTTLE (71205-285-30)Jun 1, 2019
71205-285-4040 TABLET, FILM COATED in 1 BOTTLE (71205-285-40)Nov 1, 2019
71205-285-4545 TABLET, FILM COATED in 1 BOTTLE (71205-285-45)Jun 1, 2019
71205-285-6060 TABLET, FILM COATED in 1 BOTTLE (71205-285-60)Jun 1, 2019
71205-285-9090 TABLET, FILM COATED in 1 BOTTLE (71205-285-90)Jun 1, 2019

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