Tirofiban Hydrochloride
- Product NDC
- 14789-101
- 11-digit product format
- 147890101
- Labeler code
- 14789
- Product ID
- 14789-101_2dfa5385-2e91-c26a-e063-6394a90a37aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tirofiban Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Nexus Pharmaceuticals LLC
- Application
- ANDA213947
- Marketing category
- ANDA
- Marketing start
- 2023-09-25
- Substance
- TIROFIBAN HYDROCHLORIDE
- Active strength
- 50 ug/mL
- Pharmacologic classes
- Decreased Platelet Aggregation [PE], Platelet Aggregation Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tirofiban Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TIROFIBAN HYDROCHLORIDE | 50 ug/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6H925F8O5J |
| Rxcui | 1737466, 1737471 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 14789-101-01 | Tirofiban Hydrochloride | 1 in 1 CARTON | INJECTION | 1 | | 10 |
| 14789-101-01 | Tirofiban Hydrochloride | 100 mL in 1 BAG | INJECTION | 100 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 14789-101 | TIROFIBAN HYDROCHLORIDE INJECTION [NEXUS PHARMACEUTICALS LLC] | 10 | Current NDC, 2 package rows | 20250221_7731e46a-2121-441b-b090-12dcefe240f0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 14789-101-01 | 14789010101 | 1 BAG in 1 CARTON (14789-101-01) / 100 mL in 1 BAG | 1 bag | 2023-09-25 | No | No | Historical |