NDC 25021-806

haloperidol

Haloperidol Lactate

haloperidol is a Intramuscular Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Sagent Pharmaceuticals. The primary component is Haloperidol Lactate.

Product ID25021-806_0ee8e325-6089-44b2-8882-055e1c1e3474
NDC25021-806
Product TypeHuman Prescription Drug
Proprietary Namehaloperidol
Generic NameHaloperidol Lactate
Dosage FormInjection, Solution
Route of AdministrationINTRAMUSCULAR
Marketing Start Date2011-10-24
Marketing CategoryANDA / ANDA
Application NumberANDA091637
Labeler NameSagent Pharmaceuticals
Substance NameHALOPERIDOL LACTATE
Active Ingredient Strength5 mg/mL
Pharm ClassesTypical Antipsychotic [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 25021-806-01

10 VIAL in 1 CARTON (25021-806-01) > 1 mL in 1 VIAL
Marketing Start Date2011-10-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 25021-806-01 [25021080601]

haloperidol INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA091637
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2011-10-24

Drug Details

Active Ingredients

IngredientStrength
HALOPERIDOL LACTATE5 mg/mL

OpenFDA Data

SPL SET ID:7ce7f23c-f58b-4b8b-a31a-47bd4e792345
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 204416
  • 1719646
  • Pharmacological Class

    • Typical Antipsychotic [EPC]

    Medicade Reported Pricing

    25021080601 HALOPERIDOL LAC 5 MG/ML VIAL

    Pricing Unit: ML | Drug Type:

    NDC Crossover Matching brand name "haloperidol" or generic name "Haloperidol Lactate"

    NDCBrand NameGeneric Name
    0093-9604HaloperidolHaloperidol lactate
    0121-0581HaloperidolHaloperidol
    0143-9319HaloperidolHaloperidol lactate
    0143-9501HaloperidolHaloperidol lactate
    0143-9502HaloperidolHaloperidol Lactate
    0378-0214Haloperidolhaloperidol
    0378-0257Haloperidolhaloperidol
    0378-0327Haloperidolhaloperidol
    0378-0334Haloperidolhaloperidol
    0378-0335Haloperidolhaloperidol
    0378-0351Haloperidolhaloperidol
    68083-117HaloperidolHaloperidol
    68084-250HaloperidolHaloperidol
    68084-249HaloperidolHaloperidol
    68258-7077HaloperidolHaloperidol
    68382-079HaloperidolHaloperidol
    68382-081HaloperidolHaloperidol
    68382-080HaloperidolHaloperidol
    70518-0035HaloperidolHaloperidol
    70518-0023HaloperidolHaloperidol
    70518-0728HaloperidolHaloperidol
    70518-0831HaloperidolHaloperidol
    70518-0776HaloperidolHaloperidol
    70518-1599HaloperidolHaloperidol
    70518-1182HaloperidolHaloperidol
    70518-1720HaloperidolHaloperidol
    70518-1803HaloperidolHaloperidol
    70518-1269HaloperidolHaloperidol
    70518-1529HaloperidolHaloperidol
    0615-2597HaloperidolHaloperidol
    0615-2596HaloperidolHaloperidol
    0615-2594HaloperidolHaloperidol
    0615-2598HaloperidolHaloperidol
    0615-2595HaloperidolHaloperidol
    0781-1396HaloperidolHaloperidol
    0781-1391HaloperidolHaloperidol
    0781-1392HaloperidolHaloperidol
    0781-1393HaloperidolHaloperidol
    0781-1398HaloperidolHaloperidol
    0781-1397HaloperidolHaloperidol
    0904-5925HaloperidolHaloperidol
    0904-5924HaloperidolHaloperidol
    0904-5923HaloperidolHaloperidol
    0904-6413HaloperidolHaloperidol
    10147-0911HaloperidolHaloperidol
    17856-0581HaloperidolHaloperidol
    17478-110HaloperidolHaloperidol
    21695-653HaloperidolHaloperidol
    25021-806haloperidolhaloperidol
    43063-551HaloperidolHaloperidol

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.