United States · FDA National Drug Code directory

tizanidine

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
50090-7716_9edb8ad4-7e86-4eb9-b5b9-466b466c3fe7
Product NDC
50090-7716
Form
TABLET
Composition / generic term
tizanidine
Labeler
A-S Medication Solutions
Marketing category
ANDA
Marketing start / end (source format)
20241215
Source listing expiry
20261231

Source-listed ingredients

  • TIZANIDINE HYDROCHLORIDE — 2 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (50090-7716-0) · 50090-7716-0
  • 60 TABLET in 1 BOTTLE (50090-7716-1) · 50090-7716-1

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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