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
- 80425-0454_27889dea-01b2-ed7b-e063-6394a90acbc8
- Product NDC
- 80425-0454
- Form
- TABLET
- Composition / generic term
- tizanidine
- Labeler
- Advanced Rx of Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241122
- Source listing expiry
- 20261231
Source-listed ingredients
- TIZANIDINE HYDROCHLORIDE — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (80425-0454-1) · 80425-0454-1
- 60 TABLET in 1 BOTTLE (80425-0454-2) · 80425-0454-2
- 90 TABLET in 1 BOTTLE (80425-0454-3) · 80425-0454-3
- 120 TABLET in 1 BOTTLE (80425-0454-4) · 80425-0454-4
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 →