NDC 70771-1107

Eletriptan hydrobromide

Eletriptan Hydrobromide

Eletriptan hydrobromide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Cadila Healthcare Limited. The primary component is Eletriptan Hydrobromide.

Product ID70771-1107_0cbdde4b-4f35-4a0d-90dd-90cd55b8c179
NDC70771-1107
Product TypeHuman Prescription Drug
Proprietary NameEletriptan hydrobromide
Generic NameEletriptan Hydrobromide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-07-12
Marketing CategoryANDA / ANDA
Application NumberANDA206409
Labeler NameCadila Healthcare Limited
Substance NameELETRIPTAN HYDROBROMIDE
Active Ingredient Strength20 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 Through2021-12-31

Packaging

NDC 70771-1107-0

1000 TABLET, FILM COATED in 1 BOTTLE (70771-1107-0)
Marketing Start Date2017-07-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70771-1107-3 [70771110703]

Eletriptan hydrobromide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206409
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-07-12

NDC 70771-1107-6 [70771110706]

Eletriptan hydrobromide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206409
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-07-12

NDC 70771-1107-0 [70771110700]

Eletriptan hydrobromide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206409
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-07-12

NDC 70771-1107-2 [70771110702]

Eletriptan hydrobromide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206409
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-07-12

NDC 70771-1107-4 [70771110704]

Eletriptan hydrobromide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206409
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-07-12

Drug Details

Active Ingredients

IngredientStrength
ELETRIPTAN HYDROBROMIDE20 mg/1

OpenFDA Data

SPL SET ID:481ae7d4-9e57-424a-9d07-2920954b6ddc
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 359494
  • 359493
    • UPC Code
  • 0370771110735
  • 0370771110834

    • 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 "Eletriptan hydrobromide" or generic name "Eletriptan Hydrobromide"

    NDCBrand NameGeneric Name
    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
    68382-923Eletriptan hydrobromideEletriptan hydrobromide
    68382-922Eletriptan hydrobromideEletriptan hydrobromide
    70771-1107Eletriptan hydrobromideEletriptan hydrobromide
    70771-1108Eletriptan hydrobromideEletriptan hydrobromide
    65162-042Eletriptan HydrobromideEletriptan Hydrobromide
    65162-043Eletriptan HydrobromideEletriptan Hydrobromide
    63629-8320Eletriptan HydrobromideEletriptan Hydrobromide
    0049-2330Relpaxeletriptan hydrobromide
    0049-2340Relpaxeletriptan hydrobromide
    21695-871Relpaxeletriptan hydrobromide
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