NDC 71205-068 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71205-068

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, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (6)

Package NDCDescriptionSince
71205-068-2020 TABLET, COATED in 1 BOTTLE (71205-068-20)Aug 1, 2018
71205-068-3030 TABLET, COATED in 1 BOTTLE (71205-068-30)Jul 2, 2018
71205-068-4040 TABLET, COATED in 1 BOTTLE (71205-068-40)Jul 2, 2018
71205-068-4545 TABLET, COATED in 1 BOTTLE (71205-068-45)Aug 1, 2018
71205-068-6060 TABLET, COATED in 1 BOTTLE (71205-068-60)Aug 1, 2018
71205-068-9090 TABLET, COATED in 1 BOTTLE (71205-068-90)Aug 1, 2018

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