NDC 0409-1187

Droperidol

Droperidol

Droperidol is a Intramuscular; Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Droperidol.

• Product ID: 0409-1187_1c59121b-3f29-4fa7-9e15-7de906666572
• NDC: 0409-1187
• Product Type: Human Prescription Drug
• Proprietary Name: Droperidol
• Generic Name: Droperidol
• Dosage Form: Injection, Solution
• Route of Administration: INTRAMUSCULAR; INTRAVENOUS
• Marketing Start Date: 2005-08-23
• Marketing Category: ANDA / ANDA
• Application Number: ANDA071981
• Labeler Name: Hospira, Inc.
• Substance Name: DROPERIDOL
• Active Ingredient Strength: 3 mg/mL
• Pharm Classes: Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0409-1187-01

10 AMPULE in 1 CARTON (0409-1187-01) > 2 mL in 1 AMPULE

• Marketing Start Date: 2005-08-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0409-1187-01 [00409118701]

Droperidol INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA071981
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2005-08-23

NDC 0409-1187-11 [00409118711]

Droperidol INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA071981
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2020-02-27

Drug Details

Active Ingredients

Ingredient	Strength
DROPERIDOL	2.5 mg/mL

OpenFDA Data

• SPL SET ID: b99a44df-ff38-4602-68ab-9bef1ff3af83
• Manufacturer:
  • Hospira, Inc.
• UNII:
  • O9U0F09D5X
• RxNorm Concept Unique ID - RxCUI:
  • 282485

Pharmacological Class

• Dopamine D2 Antagonists [MoA]
• Dopamine-2 Receptor Antagonist [EPC]

NDC Crossover Matching brand name "Droperidol" or generic name "Droperidol"

NDC	Brand Name	Generic Name
0143-9514	DROPERIDOL	DROPERIDOL
0143-9515	DROPERIDOL	DROPERIDOL
0409-1187	Droperidol	DROPERIDOL
0517-9702	Droperidol	Droperidol