NDC 0409-4699

PROPOFOL

Propofol

PROPOFOL is a Intravenous Injection, Emulsion in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Propofol.

Product ID0409-4699_6739d85f-7f91-4b20-a360-618fa638cbf8
NDC0409-4699
Product TypeHuman Prescription Drug
Proprietary NamePROPOFOL
Generic NamePropofol
Dosage FormInjection, Emulsion
Route of AdministrationINTRAVENOUS
Marketing Start Date2006-04-03
Marketing CategoryANDA / ANDA
Application NumberANDA077908
Labeler NameHospira, Inc.
Substance NamePROPOFOL
Active Ingredient Strength10 mg/mL
Pharm ClassesGeneral Anesthesia [PE],General Anesthetic [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0409-4699-24

10 VIAL in 1 TRAY (0409-4699-24) > 100 mL in 1 VIAL (0409-4699-54)
Marketing Start Date2006-04-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0409-4699-63 [00409469963]

PROPOFOL INJECTION, EMULSION
Marketing CategoryANDA
Application NumberANDA077908
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2010-01-06
Marketing End Date2014-08-26

NDC 0409-4699-33 [00409469933]

PROPOFOL INJECTION, EMULSION
Marketing CategoryANDA
Application NumberANDA077908
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-04-03

NDC 0409-4699-54 [00409469954]

PROPOFOL INJECTION, EMULSION
Marketing CategoryANDA
Application NumberANDA077908
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-06-20

NDC 0409-4699-50 [00409469950]

PROPOFOL INJECTION, EMULSION
Marketing CategoryANDA
Application NumberANDA077908
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-06-20

NDC 0409-4699-24 [00409469924]

PROPOFOL INJECTION, EMULSION
Marketing CategoryANDA
Application NumberANDA077908
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-04-03

NDC 0409-4699-62 [00409469962]

PROPOFOL INJECTION, EMULSION
Marketing CategoryANDA
Application NumberANDA077908
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2010-01-06
Marketing End Date2014-08-26

NDC 0409-4699-61 [00409469961]

PROPOFOL INJECTION, EMULSION
Marketing CategoryANDA
Application NumberANDA077908
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2010-01-06
Marketing End Date2014-08-26

NDC 0409-4699-53 [00409469953]

PROPOFOL INJECTION, EMULSION
Marketing CategoryANDA
Application NumberANDA077908
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-06-20

NDC 0409-4699-30 [00409469930]

PROPOFOL INJECTION, EMULSION
Marketing CategoryANDA
Application NumberANDA077908
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-04-04

Drug Details

Active Ingredients

IngredientStrength
PROPOFOL10 mg/mL

OpenFDA Data

SPL SET ID:28d7ba00-f824-4e55-139a-03f509c099db
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1808217
  • 1808224
  • 1808222
  • Pharmacological Class

    • General Anesthesia [PE]
    • General Anesthetic [EPC]

    NDC Crossover Matching brand name "PROPOFOL" or generic name "Propofol"

    NDCBrand NameGeneric Name
    0069-0209PropofolPropofol
    0069-0234PropofolPropofol
    0069-0248PropofolPropofol
    0404-9943PROPOFOLpropofol
    0409-4699PROPOFOLPROPOFOL
    0409-6010PROPOFOLPROPOFOL
    0591-2136PropofolPropofol
    0641-6194PropofolPropofol
    0641-6195PropofolPropofol
    0641-6196PropofolPropofol
    16714-528propofolpropofol
    16714-690propofolpropofol
    16714-977propofolpropofol
    23155-345propofolpropofol
    25021-608propofolpropofol
    50090-4569PropofolPropofol
    51662-1293PROPOFOLPROPOFOL
    51662-1470PROPOFOLPROPOFOL
    51662-1471PROPOFOLPROPOFOL
    52584-054PropofolPropofol
    52584-098PROPOFOLpropofol
    52584-699PropofolPropofol
    18124-027Fresenius Propoven 2%PROPOFOL

    Trademark Results [PROPOFOL]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PROPOFOL
    PROPOFOL
    90235915 not registered Live/Pending
    Twilight Co.
    2020-10-05
    PROPOFOL
    PROPOFOL
    87725806 5534295 Live/Registered
    Liu Xiaojiao
    2017-12-19

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