United States · FDA National Drug Code directory
Tirofiban hydrochloride
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
- 68083-145_a206685a-4e0d-40a1-8f39-a4b2f660d7d7
- Product NDC
- 68083-145
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Tirofiban
- Labeler
- Gland Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210415
- Source listing expiry
- 20261231
Source-listed ingredients
- TIROFIBAN HYDROCHLORIDE — 12.5 mg/250mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 CONTAINER in 1 CARTON (68083-145-01) / 250 mL in 1 CONTAINER · 68083-145-01
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 →