Relpax - 63539-234-79 - (eletriptan hydrobromide)

Alphabetical Index


Drug Information of Relpax

Product NDC: 63539-234
Proprietary Name: Relpax
Non Proprietary Name: eletriptan hydrobromide
Active Ingredient(s): 40    mg/1 & nbsp;   eletriptan hydrobromide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Relpax

Product NDC: 63539-234
Labeler Name: U.S. Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021016
Marketing Category: NDA
Start Marketing Date: 20021226

Package Information of Relpax

Package NDC: 63539-234-79
Package Description: 1 TABLET, FILM COATED in 1 BLISTER PACK (63539-234-79)

NDC Information of Relpax

NDC Code 63539-234-79
Proprietary Name Relpax
Package Description 1 TABLET, FILM COATED in 1 BLISTER PACK (63539-234-79)
Product NDC 63539-234
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name eletriptan hydrobromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20021226
Marketing Category Name NDA
Labeler Name U.S. Pharmaceuticals
Substance Name ELETRIPTAN HYDROBROMIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Complete Information of Relpax


General Information