United States · FDA National Drug Code directory

Methocarbamol

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
71335-0909_e528cb2f-d2bb-4c7a-89d2-462607df3583
Product NDC
71335-0909
Form
TABLET, COATED
Composition / generic term
Methocarbamol Tablets
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20180702
Source listing expiry
20271231

Source-listed ingredients

  • METHOCARBAMOL — 750 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 14 TABLET, COATED in 1 BOTTLE (71335-0909-0) · 71335-0909-0
  • 20 TABLET, COATED in 1 BOTTLE (71335-0909-1) · 71335-0909-1
  • 30 TABLET, COATED in 1 BOTTLE (71335-0909-2) · 71335-0909-2
  • 40 TABLET, COATED in 1 BOTTLE (71335-0909-3) · 71335-0909-3
  • 120 TABLET, COATED in 1 BOTTLE (71335-0909-4) · 71335-0909-4
  • 60 TABLET, COATED in 1 BOTTLE (71335-0909-5) · 71335-0909-5
  • 90 TABLET, COATED in 1 BOTTLE (71335-0909-6) · 71335-0909-6
  • 112 TABLET, COATED in 1 BOTTLE (71335-0909-7) · 71335-0909-7
  • 21 TABLET, COATED in 1 BOTTLE (71335-0909-8) · 71335-0909-8
  • 84 TABLET, COATED in 1 BOTTLE (71335-0909-9) · 71335-0909-9

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →