NDC 0143-9514

DROPERIDOL

Droperidol

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

Product ID0143-9514_a7e520ca-3213-4203-9a23-5295d82088e3
NDC0143-9514
Product TypeHuman Prescription Drug
Proprietary NameDROPERIDOL
Generic NameDroperidol
Dosage FormInjection, Solution
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS
Marketing Start Date2022-06-01
Marketing CategoryANDA /
Application NumberANDA208197
Labeler NameHikma Pharmaceuticals USA Inc.
Substance NameDROPERIDOL
Active Ingredient Strength3 mg/mL
Pharm ClassesDopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0143-9514-25

25 VIAL in 1 CARTON (0143-9514-25) > 2 mL in 1 VIAL (0143-9514-01)
Marketing Start Date2022-06-01
NDC Exclude FlagN
Sample Package?N

Drug Details

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

NDCBrand NameGeneric Name
0143-9514DROPERIDOLDROPERIDOL
0143-9515DROPERIDOLDROPERIDOL
0409-1187DroperidolDROPERIDOL
0517-9702DroperidolDroperidol

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