NDC 63539-234

Relpax

Eletriptan Hydrobromide

Relpax is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by U.s. Pharmaceuticals. The primary component is Eletriptan Hydrobromide.

Product ID63539-234_4fdc09b8-7aa8-437f-b664-8daecfe92851
NDC63539-234
Product TypeHuman Prescription Drug
Proprietary NameRelpax
Generic NameEletriptan Hydrobromide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2002-12-26
Marketing CategoryNDA / NDA
Application NumberNDA021016
Labeler NameU.S. Pharmaceuticals
Substance NameELETRIPTAN HYDROBROMIDE
Active Ingredient Strength40 mg/1
Pharm ClassesSerotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 63539-234-45

6 BLISTER PACK in 1 CARTON (63539-234-45) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2002-12-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63539-234-96 [63539023496]

Relpax TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021016
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-12-26

NDC 63539-234-45 [63539023445]

Relpax TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021016
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-12-26

NDC 63539-234-79 [63539023479]

Relpax TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021016
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-12-26

Drug Details

Active Ingredients

IngredientStrength
ELETRIPTAN HYDROBROMIDE40 mg/1

OpenFDA Data

SPL SET ID:986dc112-b97b-44a3-bfaf-074f906f8bb2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 359494
  • 404444
  • Pharmacological Class

    • Serotonin 1b Receptor Agonists [MoA]
    • Serotonin 1d Receptor Agonists [MoA]
    • Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

    NDC Crossover Matching brand name "Relpax" or generic name "Eletriptan Hydrobromide"

    NDCBrand NameGeneric Name
    0049-2330Relpaxeletriptan hydrobromide
    0049-2340Relpaxeletriptan hydrobromide
    21695-871Relpaxeletriptan hydrobromide
    63539-234RelpaxRelpax
    0093-8310Eletriptan HydrobromideEletriptan Hydrobromide
    0093-8311Eletriptan HydrobromideEletriptan Hydrobromide
    0378-4287Eletriptan Hydrobromideeletriptan hydrobromide
    0378-4288Eletriptan Hydrobromideeletriptan hydrobromide
    27241-039eletriptan hydrobromideeletriptan hydrobromide
    27241-040eletriptan hydrobromideeletriptan hydrobromide
    55700-756eletriptan hydrobromideeletriptan hydrobromide
    59651-104Eletriptan HydrobromideEletriptan Hydrobromide
    59651-105Eletriptan HydrobromideEletriptan Hydrobromide

    Trademark Results [Relpax]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    RELPAX
    RELPAX
    75655002 2747535 Dead/Cancelled
    Pfizer Inc.
    1999-03-05
    RELPAX
    RELPAX
    75249087 2487796 Live/Registered
    Pfizer Inc.
    1997-02-27

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