NDC 70518-1720

Haloperidol

Haloperidol

Haloperidol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Haloperidol.

Product ID70518-1720_7cc82eea-723f-8aed-e053-2a91aa0a0a49
NDC70518-1720
Product TypeHuman Prescription Drug
Proprietary NameHaloperidol
Generic NameHaloperidol
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-12-07
Marketing CategoryANDA / ANDA
Application NumberANDA070278
Labeler NameREMEDYREPACK INC.
Substance NameHALOPERIDOL
Active Ingredient Strength5 mg/1
Pharm ClassesTypical Antipsychotic [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 70518-1720-0

30 TABLET in 1 BLISTER PACK (70518-1720-0)
Marketing Start Date2018-12-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-1720-0 [70518172000]

Haloperidol TABLET
Marketing CategoryANDA
Application NumberANDA070278
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-12-07
Marketing End Date2020-05-28

Drug Details

Active Ingredients

IngredientStrength
HALOPERIDOL5 mg/1

OpenFDA Data

SPL SET ID:8634f952-685b-4251-a9f4-9185deadd219
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310672
  • Pharmacological Class

    • Typical Antipsychotic [EPC]

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

    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.