United States · FDA National Drug Code directory

ATMEKSI

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
69528-701_4ce9560d-185c-1e28-e063-6294a90af77f
Product NDC
69528-701
Form
SUSPENSION
Composition / generic term
methocarbamol
Labeler
Rosemont Pharmaceuticals LLC
Marketing category
NDA
Marketing start / end (source format)
20251222
Source listing expiry
20271231

Source-listed ingredients

  • METHOCARBAMOL — 750 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 150 mL in 1 BOTTLE (69528-701-05) · 69528-701-05

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.

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