droperidol

Generic: droperidol

Labeler: american regent, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name droperidol
Generic Name droperidol
Labeler american regent, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

droperidol 2.5 mg/mL

Manufacturer
American Regent, Inc.

Identifiers & Regulatory

Product NDC 0517-9702
Product ID 0517-9702_8bcdfec0-1df7-413d-82c1-ac564d18aaa0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072123
Listing Expiration 2026-12-31
Marketing Start 1990-09-30

Pharmacologic Class

Established (EPC)
dopamine-2 receptor antagonist [epc]
Mechanism of Action
dopamine d2 antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05179702
Hyphenated Format 0517-9702

Supplemental Identifiers

RxCUI
282485
UPC
0305179702251
UNII
O9U0F09D5X
NUI
N0000175799 N0000175800

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 droperidol (source: ndc)
Generic Name droperidol (source: ndc)
Application Number ANDA072123 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-9702-25) / 2 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

droperidol (2.5 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "8bcdfec0-1df7-413d-82c1-ac564d18aaa0", "openfda": {"nui": ["N0000175799", "N0000175800"], "upc": ["0305179702251"], "unii": ["O9U0F09D5X"], "rxcui": ["282485"], "spl_set_id": ["147e033d-d997-4ef6-8bb5-a9ba372590b2"], "pharm_class_epc": ["Dopamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Dopamine D2 Antagonists [MoA]"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0517-9702-25)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0517-9702-25", "marketing_start_date": "19900930"}], "brand_name": "Droperidol", "product_id": "0517-9702_8bcdfec0-1df7-413d-82c1-ac564d18aaa0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0517-9702", "generic_name": "Droperidol", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Droperidol", "active_ingredients": [{"name": "DROPERIDOL", "strength": "2.5 mg/mL"}], "application_number": "ANDA072123", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}