NDC 42023-196

Corphedra

Ephedrine Sulfate

Corphedra is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Par Pharmaceutical, Inc.. The primary component is Ephedrine Sulfate.

Product ID42023-196_2f07b040-7bb7-4587-9aa0-8f826306f346
NDC42023-196
Product TypeHuman Prescription Drug
Proprietary NameCorphedra
Generic NameEphedrine Sulfate
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2017-02-16
Marketing CategoryNDA / NDA
Application NumberNDA208943
Labeler NamePar Pharmaceutical, Inc.
Substance NameEPHEDRINE SULFATE
Active Ingredient Strength50 mg/mL
Pharm Classesalpha-Adrenergic Agonist [EPC],Adrenergic alpha-Agonists [MoA],beta-Adrenergic Agonist [EPC],Adrenergic beta-Agonists [MoA],Norepinephrine Releasing Agent [EPC],Increased Norepinephrine Activity [PE]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 42023-196-25

25 VIAL in 1 CARTON (42023-196-25) > 1 mL in 1 VIAL (42023-196-01)
Marketing Start Date2017-02-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 42023-196-01 [42023019601]

Corphedra INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA208943
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-16

NDC 42023-196-25 [42023019625]

Corphedra INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA208943
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-16

Drug Details

Active Ingredients

IngredientStrength
EPHEDRINE SULFATE50 mg/mL

OpenFDA Data

SPL SET ID:98531820-a85c-4ee7-9338-2be264219afe
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1116294
  • 1870691

    • Pharmacological Class

    • alpha-Adrenergic Agonist [EPC]
    • Adrenergic alpha-Agonists [MoA]
    • beta-Adrenergic Agonist [EPC]
    • Adrenergic beta-Agonists [MoA]
    • Norepinephrine Releasing Agent [EPC]
    • Increased Norepinephrine Activity [PE]

    NDC Crossover Matching brand name "Corphedra" or generic name "Ephedrine Sulfate"

    NDCBrand NameGeneric Name
    42023-196CorphedraEphedrine Sulfate
    42023-233Corphedraephedrine sulfate
    14789-250EmerphedEphedrine Sulfate
    0143-3145Ephedrine SulfateEphedrine Sulfate
    0363-5789Ephedrine SulfateEphedrine Sulfate
    0641-6238Ephedrine SulfateEphedrine Sulfate
    0781-3269Ephedrine SulfateEphedrine Sulfate
    14789-014Ephedrine SulfateEphedrine Sulfate
    16714-037Ephedrine SulfateEphedrine Sulfate
    17478-415Ephedrine SulfateEphedrine Sulfate
    17478-515Ephedrine SulfateEphedrine Sulfate
    17478-517Ephedrine SulfateEphedrine Sulfate
    17478-955Ephedrine SulfateEphedrine Sulfate
    42023-216Ephedrine SulfateEphedrine Sulfate
    42023-243EPHEDRINE SULFATEEphedrine Sulfate
    42023-253EPHEDRINE SULFATEEphedrine Sulfate
    43598-725Ephedrine sulfateEphedrine sulfate

    Trademark Results [Corphedra]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    CORPHEDRA
    CORPHEDRA
    86921301 not registered Dead/Abandoned
    PAR PHARMACEUTICAL, INC.
    2016-02-26
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