NDC 59651-105 – Eletriptan Hydrobromide

Eletriptan Hydrobromide 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC59651-105

Product details

Brand name
Eletriptan Hydrobromide
Generic name
Eletriptan Hydrobromide
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210708
Marketed since
February 16, 2018
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-1b and Serotonin-1d Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Eletriptan hydrobromide →

Package NDC codes (2)

Package NDCDescriptionSince
59651-105-691 BLISTER PACK in 1 CARTON (59651-105-69) / 6 TABLET, FILM COATED in 1 BLISTER PACK (59651-105-06)Jan 15, 2019
59651-105-932 BLISTER PACK in 1 CARTON (59651-105-93) / 6 TABLET, FILM COATED in 1 BLISTER PACKJan 15, 2019

Recalls mentioning this NDC

Other Eletriptan hydrobromide products