tirofiban hydrochloride

Generic: tirofiban hydrochloride

Labeler: nexus pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tirofiban hydrochloride
Generic Name tirofiban hydrochloride
Labeler nexus pharmaceuticals llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

tirofiban hydrochloride 50 ug/mL

Manufacturer
Nexus Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 14789-102
Product ID 14789-102_2dfa5385-2e91-c26a-e063-6394a90a37aa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213947
Listing Expiration 2026-12-31
Marketing Start 2023-09-25

Pharmacologic Class

Classes
decreased platelet aggregation [pe] platelet aggregation inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 14789102
Hyphenated Format 14789-102

Supplemental Identifiers

RxCUI
1737466 1737471
UNII
6H925F8O5J

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name tirofiban hydrochloride (source: ndc)
Generic Name tirofiban hydrochloride (source: ndc)
Application Number ANDA213947 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 ug/mL
source: ndc
Packaging
  • 1 BAG in 1 CARTON (14789-102-02) / 250 mL in 1 BAG
  • 2 BAG in 1 CARTON (14789-102-10) / 250 mL in 1 BAG
source: ndc

Packages (2)

14789-102-02 1 BAG in 1 CARTON (14789-102-02) / 250 mL in 1 BAG 14789-102-10 2 BAG in 1 CARTON (14789-102-10) / 250 mL in 1 BAG

Ingredients (1)

tirofiban hydrochloride (50 ug/mL)

Linked Drug Pages (1)

Tirofiban Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2dfa5385-2e91-c26a-e063-6394a90a37aa", "openfda": {"unii": ["6H925F8O5J"], "rxcui": ["1737466", "1737471"], "spl_set_id": ["7731e46a-2121-441b-b090-12dcefe240f0"], "manufacturer_name": ["Nexus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 CARTON (14789-102-02)  / 250 mL in 1 BAG", "package_ndc": "14789-102-02", "marketing_start_date": "20230925"}, {"sample": false, "description": "2 BAG in 1 CARTON (14789-102-10)  / 250 mL in 1 BAG", "package_ndc": "14789-102-10", "marketing_start_date": "20240210"}], "brand_name": "Tirofiban Hydrochloride", "product_id": "14789-102_2dfa5385-2e91-c26a-e063-6394a90a37aa", "dosage_form": "INJECTION", "pharm_class": ["Decreased Platelet Aggregation [PE]", "Platelet Aggregation Inhibitor [EPC]"], "product_ndc": "14789-102", "generic_name": "Tirofiban Hydrochloride", "labeler_name": "Nexus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tirofiban Hydrochloride", "active_ingredients": [{"name": "TIROFIBAN HYDROCHLORIDE", "strength": "50 ug/mL"}], "application_number": "ANDA213947", "marketing_category": "ANDA", "marketing_start_date": "20230925", "listing_expiration_date": "20261231"}